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ChemicalBook CAS DataBase List 2-Butyne

2-Butyne synthesis

5synthesis methods
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Yield:501-65-5 99%

Reaction Conditions:

with Mo(≡N)(OSiPh3)3(phen);manganese(ll) chloride in toluene at 80; for 3.5 h;Schlenk technique;Inert atmosphere;Molecular sieve;Reagent/catalyst;

Steps:

I.11 11. Alkyne Metathesis by Activation of [Mo(≡N)(OSiPh3)3(Phen)] by Means of MnCl2 Prior to the Addition of the Substrate
11. Alkyne Metathesis by Activation of [Mo(≡N)(OSiPh3)3(Phen)] by Means of MnCl2 Prior to the Addition of the Substrate
In a dry 25 mL Schlenk-tube, which has been flooded with argon, [Mo(≡N)(OSiPh3)3(phen)].0.5 toluene (0.100 mmol, 116.2 mg), MnCl2 (0.100 mmol, 12.6 mg) and molecular sieve (1.00 g, 5Å, powder) were suspended in 5 mL of toluene and the mixture was heated to 80° C. After 30 min 1-penyl-1-propine (1.00 mmol, 116.2 mg) were added, the reaction mixture was stirred for 3 h at 80° C. and was filtered after cooling over a short silica gel column. The filtrate was concentrated and the residue was purified by column chromatography (hexane). 88.2 mg of tolane (99%) were isolated as white solid, the spectroscopic and analytical data of which were identical to those of a commercial sample. M.p.=59-61° C

References:

Studiengesellschaft Kohle mbH;Fuerstner, Alois;Heppekausen, Johannes;Hickmann, Volker;Stade, Robert US8993470, 2015, B2 Location in patent:Page/Page column 36; 37; 47; 48

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