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Water → (Z)-3-(4-bromo-phenyl)-3-phenyl-prop-2-en-1-ol

HRID 984948
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HRID 984948 반응식
CC(C[AlH]CC(C)C)C.C1(C)C=CC=CC=1.C([O:19][C:20](=O)/[CH:21]=[C:22](\[C:29]1[CH:34]=[CH:33][C:32]([Br:35])=[CH:31][CH:30]=1)/[C:23]1[CH:28]=[CH:27][CH:26]=[CH:25][CH:24]=1)C.O>C1COCC1>[Br:35][C:32]1[CH:31]=[CH:30][C:29](/[C:22](/[C:23]2[CH:24]=[CH:25][CH:26]=[CH:27][CH:28]=2)=[CH:21]\[CH2:20][OH:19])=[CH:34][CH:33]=1
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

6

반응물 4

HCID 962WaterHCID 1140TolueneHCID 14487Diisobutylaluminum hydrideHCID 11067512(Z)-3-(4-bromo-phenyl)-3-phenyl-acrylic acid ethyl ester

생성물 1

HCID 22270289(Z)-3-(4-bromo-phenyl)-3-phenyl-prop-2-en-1-ol수율 96%

시약·촉매·용매 1

HCID 8028
Tetrahydrofuran
용매

실험 절차

A 1.2 M solution of DIBAL-H in toluene (84 ml, 100 mmol) was added dropwise, at −15° C. over 20 min, to a stirred solution of (Z)-3-(4-bromophenyl)-3-phenylacrylicacid ethyl ester (11.1 g, 33.5 mmol) in dry THF (150 ml), and the mixture stirred for 30 min. Rochelles salt and water was carefully added, and the resulting mixture extracted with ethyl acetate (x2). The combined organic extracts were washed with brine, dried (MgSO4), and evaporated to give 9.3 g of (Z)-3-(4-bromo-phenyl)-3-phenyl-prop-2-en-1-ol.

후처리

  1. extractionthe resulting mixture extracted with ethyl acetate (x2)
  2. washThe combined organic extracts were washed with brine
  3. dry with materialdried (MgSO4)
  4. customevaporated

출처 및 근거

ORD 기록
ord-e60552c2877a4f90af68a9ba47e00d24
출처 데이터셋
uspto-grants-2005_03
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US06869967B2

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