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Boron tribromide → 3-Cyclohexyl-1-(2,6-dichloro-4-hydroxy-benzyl)-pyrrolidin-2-one

HRID 1670837
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HRID 1670837 반응식
[CH:1]1([CH:7]2[CH2:11][CH2:10][N:9]([CH2:12][C:13]3[C:18]([Cl:19])=[CH:17][C:16]([O:20]C)=[CH:15][C:14]=3[Cl:22])[C:8]2=[O:23])[CH2:6][CH2:5][CH2:4][CH2:3][CH2:2]1.B(Br)(Br)Br>ClC(Cl)C>[CH:1]1([CH:7]2[CH2:11][CH2:10][N:9]([CH2:12][C:13]3[C:18]([Cl:19])=[CH:17][C:16]([OH:20])=[CH:15][C:14]=3[Cl:22])[C:8]2=[O:23])[CH2:2][CH2:3][CH2:4][CH2:5][CH2:6]1
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참가 물질

4

반응물 2

HCID 25134Boron tribromideHCID 576580123-Cyclohexyl-1-(2,6-dichloro-4-methoxy-benzyl)-pyrrolidin-2-one

생성물 1

HCID 576579983-Cyclohexyl-1-(2,6-dichloro-4-hydroxy-benzyl)-pyrrolidin-2-one수율 99%

시약·촉매·용매 1

HCID 63651,1-Dichloroethane용매

실험 절차

Treat a solution of 3-cyclohexyl-1-(2,6-dichloro-4-methoxy-benzyl)-pyrrolidin-2-one (1.3 g, 3.66 mmol) in dichloroethane (30 mL) at −20° C. with boron tribromide (1.0 M in DCM, 18.3 mL) for 2 hours. Warm the reaction up to room temperature and stir for 12 hours. Quench the reaction with methanol and remove the solvent under vacuum. Partition the residue with ethyl acetate and HCl (1 N). Wash the organic with water. After drying the organic layer, filtrate and concentrate to afford 1.2 g (99%) of the title compound. MS (m/z): 342 (M+).

후처리

  1. temperatureWarm
  2. customthe reaction up to room temperature
  3. customQuench
  4. customthe reaction with methanol
  5. customremove the solvent under vacuum
  6. customPartition the residue with ethyl acetate and HCl (1 N)
  7. washWash the organic with water
  8. customAfter drying the organic layer, filtrate
  9. concentrationconcentrate

출처 및 근거

ORD 기록
ord-c559225c42224dd398c353ab9f7ab4c9
출처 데이터셋
uspto-grants-2011_08
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US07994176B2

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