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Propylene Oxide → 1-(4-Chlorophenyl)propan-2-ol

HRID 912029
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HRID 912029 반응식
[Cl:1][C:2]1[CH:7]=[CH:6][C:5]([Mg]Br)=[CH:4][CH:3]=1.[CH2:10]1[O:13][CH:11]1[CH3:12]>CCOCC.C1COCC1>[Cl:1][C:2]1[CH:7]=[CH:6][C:5]([CH2:10][CH:11]([OH:13])[CH3:12])=[CH:4][CH:3]=1
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참가 물질

5

반응물 2

HCID 6378Propylene OxideHCID 178478191HCID 178478191, 화합물

생성물 1

HCID 124998511-(4-Chlorophenyl)propan-2-ol

시약·촉매·용매 2

HCID 3283Diethyl Ether용매HCID 8028Tetrahydrofuran용매2회

실험 절차

General Procedure FF: To a THF (5 mL) solution of 1.0 M of 4-chlorophenylmagnesium bromide in Et2O (10.0 mL) was added a solution of propylene oxide (0.87 g, 15 mmol) in THF (5 mL) at −78° C. under nitrogen and stirred. The mixture was slowly warmed to rt. The mixture was quenched with sat. aq NH4Cl (10 mL) and then extracted with EtOAc (50 mL). The organic phase was washed with brine (10 mL) and dried over anhydrous sodium sulfate. The crude material was purified by silica gel chromatography using Hexane/EtOAc (80:20) as eluent to give the desired product as a colorless oil. 1H NMR (CDCl3, 400 MHz): δ=1.23-1.26 (m, 3H), 1.44 (d, J=3.8 Hz, 1H), 2.65-2.80 (m, 2H), 3.97-4.07 (m, 1H), 7.14-7.18 (m, 2H), 7.28-7.32 (m, 2H).

후처리

  1. customThe mixture was quenched with sat. aq NH4Cl (10 mL)
  2. extractionextracted with EtOAc (50 mL)
  3. washThe organic phase was washed with brine (10 mL)
  4. dry with materialdried over anhydrous sodium sulfate
  5. customThe crude material was purified by silica gel chromatography

출처 및 근거

ORD 기록
ord-c18e1662fb3342fab2f591260b13d0bd
출처 데이터셋
uspto-grants-2011_09
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08022206B2

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