반응 #502111

ord-7ab72a1b4004402e9802876b8ec4acd9

반응 방정식

CC1(C)OC[C@@H](CO)O1
((4R)-2,2-dimethyl-1,3-dioxolan-4-yl)methan-1-ol
CCN(CC)CC
triethylamine
CC(C)(C)[Si](Cl)(c1ccccc1)c1ccccc1
tert-butylchlorodiphenylsilane
CC1(C)OC[C@@H](CO[Si](c2ccccc2)(c2ccccc2)C(C)(C)C)O1
title compound
수율 106.2%
CC1(C)OC[C@@H](CO[Si](c2ccccc2)(c2ccccc2)C(C)(C)C)O1
1-(((4S)-2,2-Dimethyl(1,3-dioxolan-4-yl))methoxy)-2,2-dimethyl-1,1-diphenyl-1-silapropane
수율 106.2%

반응 조건

상세 조건
See reaction.notes.procedure_details.

후처리

  1. 1
    세척the reaction mixture was washed with water, brine
  2. 2
    건조dried over sodium sulfate
  3. 3
    여과filtered
  4. 4
    기타evaporated

실험 절차

To a solution of ((4R)-2,2-dimethyl-1,3-dioxolan-4-yl)methan-1-ol (9 g, 68.6 mmol) in anhydrous dichloromethane (40 mL) were added triethylamine (11.2 mL), tert-butylchlorodiphenylsilane (19.8 g, 372 mmol), and N,N-dimethylaminopyridine (DMAP, 418 mg, 3.4 mmol) at room temperature under a nitrogen atmosphere. The reaction mixture was stirred at room temperature overnight. It was then diluted with additional dichloromethane and the reaction mixture was washed with water, brine, dried over sodium sulfate, filtered and evaporated to give the title compound (27 g) which was used in the next step without further purification.

출처

DOI: 10.6084/m9.figshare.5104873.v1특허: US08088762B2uspto-grants-2012_01