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Triethylsilane

CAS No.
617-86-7
Chemical Name:
Triethylsilane
Synonyms
Et3SiH;Triethylsilyl;Triethylsilyl hydride;PDFF;Silane, triethyl-;Medetomidine Impurity 40;DK845;CT2523;NSC 93579;SILANE E3H
CBNumber:
CB8495938
Molecular Formula:
C6H16Si
Molecular Weight:
116.28
MDL Number:
MFCD00009018
MOL File:
617-86-7.mol
MSDS File:
SDS
Last updated:2024-11-21 17:11:28

Triethylsilane Properties

Melting point -157°C
Boiling point 107-108 °C (lit.)
Density 0.728 g/mL at 25 °C (lit.)
vapor pressure >1 hPa (20 °C)
refractive index n20/D 1.412(lit.)
Flash point 25 °F
storage temp. Store below +30°C.
solubility insol H2O; sol hydrocarbons, halocarbons, ethers.
form liquid
Specific Gravity 0.728
color colorless
Water Solubility Miscible with water.
Hydrolytic Sensitivity 3: reacts with aqueous base
Sensitive Moisture Sensitive
BRN 1098278
Stability Stable, but moisture sensitive. Highly flammable. Generates highly flammable gas (hydrogen) in contact with water, acids and bases.
LogP 3.6 at 20℃
CAS DataBase Reference 617-86-7(CAS DataBase Reference)
FDA UNII 0F9429873L
NIST Chemistry Reference Silane, triethyl-(617-86-7)
EPA Substance Registry System Triethylsilane (617-86-7)

SAFETY

Risk and Safety Statements

Symbol(GHS)  GHS hazard pictogramsGHS hazard pictograms
GHS02,GHS07
Signal word  Danger
Hazard statements  H225-H315-H319-H335
Precautionary statements  P210-P233-P240-P241-P303+P361+P353-P305+P351+P338
Hazard Codes  F,Xi
Risk Statements  11-36/37/38-52/53
Safety Statements  9-16-29-33-37/39-26-61
RIDADR  UN 1993 3/PG 2
WGK Germany  1
10-21
TSCA  Yes
HazardClass  3
PackingGroup  II
HS Code  29310095
NFPA 704
3
2 1

Triethylsilane price More Price(39)

Manufacturer Product number Product description CAS number Packaging Price Updated Buy
Sigma-Aldrich 8.18806 Triethylsilane for synthesis 617-86-7 10ML $71.1 2024-03-01 Buy
Sigma-Aldrich 8.18806 Triethylsilane for synthesis 617-86-7 50ML $179 2024-03-01 Buy
Sigma-Aldrich 230197 Triethylsilane 99% 617-86-7 5g $35.1 2024-03-01 Buy
Sigma-Aldrich 230197 Triethylsilane 99% 617-86-7 25g $89.7 2024-03-01 Buy
TCI Chemical T0662 Triethylsilane >98.0%(GC) 617-86-7 25mL $45 2024-03-01 Buy
Product number Packaging Price Buy
8.18806 10ML $71.1 Buy
8.18806 50ML $179 Buy
230197 5g $35.1 Buy
230197 25g $89.7 Buy
T0662 25mL $45 Buy

Triethylsilane Chemical Properties,Uses,Production

Description

Triethylsilane is a useful versatile reductant since it has a active hydride. It can be used for mediated the palladium-catalyzed dehalogenation reaction of alkyl or aryl halides, the reduction of primary, secondary, and tertiary chlorides, bromides, and iodides catalyzed by iridium, as well as efficient reduction of multiple bonds, azides, imines, and nitro groups, as well as benzyl group and allyl group deprotection. It is also specifically for the hydrosilation of olefins to give alkyl silanes. It is also the catalyst for synthesis of a spiro-oxindole blocker of Nav1.7 for the treatment of pain, redox initiated cationic polymerization and Beckmann rearrangement of cyclododecanone oxime as well as regioselective reductive coupling of enones and allenes.

Chemical Properties

Clear liquid

Uses

Triethylsilane serves as an exemplar for organosilicon hydride behavior as a mild reducing agent. It is frequently chosen as a synthetic reagent because of its availability, convenient physical properties, and economy relative to other organosilicon hydrides which might otherwise be suitable for effecting specific chemical transformations.
This reagent is generally used in these reactions: Hydrosilylations, Silane Alcoholysis, Formation of Singlet Oxygen, Reduction of Acyl Derivatives to Aldehydes, Radical Chain Reductions, Ionic Hydrogenations and Reductive Substitutions(The polar nature of the Si–H bond enables triethylsilane to act as a hydride donor to electron-deficient centers.), Reductive Etherifications and Acetal Reductions, Ether Cleavages, Reductive Couplings and Cyclizations, Aromatic Silylations, Generation of Other Triethylsilyl Reagents, etc.
Related Reagents: Phenylsilane–cesium fluoride; tri-n-butylstannane; tricarbonylchloroiridium–diethyl(methyl) silane–carbon monoxide; triethylsilane–trifluoroacetic acid.

Uses

Triethylsilane is a trialkylsilicon hydride used in the synthesis of alkylsilanes via hydrosilation of olefins. It acts as a reducing agent in the reduction of 2-chromanols, since it has an active hydride. It acts as a catalyst for redox initiated cationic polymerization, regioselective reductive coupling of enones and allenes, and Beckmann rearrangement of cyclododecanone oxime. It is associated with trifluoroacetic acid and involved in the selective reduction of alkenes.

Definition

ChEBI: Triethylsilane is an organosilicon compound. It has a role as a reducing agent.

Application

Triethylsilane is used as a reducing agent inmany organic synthetic reactions.
Used to reduce metal salts. Enhances deprotection of t-butoxycarbonyl-protected amines and tert-butylesters.
Used in the reductive amidation of oxazolidinones with amino acids to provide dipeptides.
Converts aldehydes to symmetrical and unsymmetrical ethers.
Used in the "in-situ" preparation of diborane and haloboranes.

Production Methods

A synthetic method of triethylsilane comprises the following steps: reacting sodium hydride with trimethyl borate to prepare trimethoxy sodium borohydride; adding triethylchlorosilane to trimethoxy sodium monohydroborate to react to obtain triethylsilane.
To a 500ml reaction flask, 20g (0.5mol) of 60% sodium hydride and 80g of anhydrous tetrahydrofuran were added. Stirring and cooling to 0-10 ℃ under the protection of nitrogen, the mixture was then maintained under nitrogen protection, stirred, and the liquid temperature at 0-10 ℃, and dropwise added 57.2g (0.55mol) of trimethyl borate. After the dropwise addition, the temperature was kept at 0-10 ℃ and stirred for 1 hour.Maintaining the nitrogen protection, stirring and liquid temperature of the reaction liquid at 0-10 ℃, and then dropwise adding 67.7g (0.45mol) of triethylchlorosilane. After the dropwise addition, continuously keep the temperature at 0-10 ℃ and stir for 1 hour. The reaction solution was then filtered at room temperature. Rectifying the filtrate at normal pressure and collecting fractions with the boiling range of 109-110 ℃ as triethylsilane to obtain 46.1g of triethylsilane, which yields 88.2%. 45-64 ℃: a mixed solution of trimethyl borate and tetrahydrofuran; 64-109 ℃:a mixture of tetrahydrofuran and a small triethylsilane.

Fire Hazard

Highly flammable; flash point -4°C (25°F) (Aldrich 1996).
It does not ignite spontaneously in air, but it can explode on heating. The ease of oxidation of this compound is relatively lower than mono- and dialkylsilanes. Reaction with oxidizing substances, however, can be violent. Reaction with boron trichloride could be explosive at room temperature. Even at 78°C ( 108°F), mixing these reagents caused pressure buildup and combustion (Matteson 1990).

Flammability and Explosibility

Flammable

Purification Methods

Reflux triethylsilane over molecular sieves, then distil it. It is passed through neutral alumina before use [Randolph & Wrighton J Am Chem Soc 108 3366 1986]. [Beilstein 4 IV 3895.]

Precautions

Triethylsilane is a flammable, but not pyrophoric, liquid. As with all organosilicon hydrides, it is capable of releasing hydrogen gas upon storage, particularly in the presence of acids, bases, or fluoride-releasing salts. Proper precautions should be taken to vent possible hydrogen buildup when opening vessels in which triethylsilane is stored.

References

R. Boukherroub,?,?, C. Chatgilialoglu,,§ and, and G. Manuel?. "PdCl2-Catalyzed Reduction of Organic Halides by Triethylsilane." Organometallics 15.5(1996):1508-1510.
Jian Yang and, and M. Brookhart. "Iridium-Catalyzed Reduction of Alkyl Halides by Triethylsilane." Journal of the American Chemical Society 129.42(2007):12656-7.
And, Pijus K. Mandal, and J. S. Mcmurray. "Pd?C-Induced Catalytic Transfer Hydrogenation with Triethylsilane." Journal of Organic Chemistry 72.17(2007):6599-6601.
Chen, Bang Chi, et al. "Novel triethylsilane mediated reductive N -alkylation of amines: improved synthesis of 1-(4-imidazolyl)methyl-4-sulfonylbenzodiazepines, new farnesyltransferase inhibitors." Tetrahedron Letters 42.7(2001):1245-1246.

994-30-9
617-86-7
Synthesis of Triethylsilane from Chlorotriethylsilane
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Triethylsilane pictures 2024-11-27 Triethylsilane
617-86-7
US $120.00 / kg 1kg 99% 10ton Hebei Zhuanglai Chemical Trading Co.,Ltd
Triethylsilane pictures 2024-11-27 Triethylsilane
617-86-7
US $0.00 / KG 1KG 98%min 30tons/month WUHAN FORTUNA CHEMICAL CO., LTD
Triethylsilane pictures 2024-11-27 Triethylsilane
617-86-7
US $0.00 / kg 1kg 99 20 tons Hubei Changfu Chemical Co., Ltd.
  • Triethylsilane pictures
  • Triethylsilane
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  • 99%
  • Hebei Zhuanglai Chemical Trading Co.,Ltd
  • Triethylsilane pictures
  • Triethylsilane
    617-86-7
  • US $0.00 / KG
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  • WUHAN FORTUNA CHEMICAL CO., LTD
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  • Triethylsilane
    617-86-7
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  • Hubei Changfu Chemical Co., Ltd.
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