N-CYCLOHEXYLHYDROXYLAMINE

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Company Name: Aurora Fine Chemicals Ltd.  
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Email: aurora@aurorafinechemicals.com
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Company Name: Riedel-de Haen AG  
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N-CYCLOHEXYLHYDROXYLAMINE Basic information
Product Name:N-CYCLOHEXYLHYDROXYLAMINE
Synonyms:N-CYCLOHEXYLHYDROXYLAMINE;AURORA KA-7611
CAS:
MF:C6H13NO
MW:115.17
EINECS:
Product Categories:
Mol File:Mol File
N-CYCLOHEXYLHYDROXYLAMINE Structure
N-CYCLOHEXYLHYDROXYLAMINE Chemical Properties
Melting point 139-140 °C(lit.)
Safety Information
Hazard Codes Xn
Risk Statements 22-41
Safety Statements 26-39
WGK Germany 2
RTECS NC3410400
MSDS Information
ProviderLanguage
SigmaAldrich English
N-CYCLOHEXYLHYDROXYLAMINE Usage And Synthesis
PreparationIn a three-necked, 50 ml flask equipped with a magnetic stirrer, thermo­meter, condenser with provision for the venting of hydrogen, and a serum cap, and containing 2.26 gm (0.02 mole) of cyclohexanone oxime at 0°C is added by means of a hypodermic syringe 17 ml of a 2 Μ solution of diborane in tetrahydrofuran at such a rate that the reaction temperature is always maintained below 10°C. After the addition has been completed, the reaction is continued for 4 hr at room temperature. Then the solvent is removed under reduced pressure and the flask's content is cooled to 0°C. By means of a syringe a few drops of 10% aqueous sodium hydroxide is added slowly.
Preparation of N-Cyclohexylhydroxylamine
CAUTION: Considerable heat may evolve at this point. In one case, a mild explosion has been reported.
Then a total of 10 ml of 10% aqueous sodium hydroxide is added. The reaction mixture is then refluxed for 1 hr and the product is separated from the reaction mixture by a 90 hr continuous extraction with pentane. The pentane solution is evaporated in a nitrogen stream to give a crude residue which sublimes at 60°C/1 mm Hg to afford 1.89 gm (82%), m.p. 140°C.
Synthesis Reference(s)The Journal of Organic Chemistry, 54, p. 4026, 1989 DOI: 10.1021/jo00278a009
N-CYCLOHEXYLHYDROXYLAMINE Preparation Products And Raw materials
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