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Sodium borohydride → 1-(4-Chloro-3-(methylsulfonyl)phenyl)ethanol

HRID 1845144
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HRID 1845144 반응식
[Cl:1][C:2]1[CH:7]=[CH:6][C:5]([C:8](=[O:10])[CH3:9])=[CH:4][C:3]=1[S:11]([CH3:14])(=[O:13])=[O:12].[BH4-].[Na+]>O1CCCC1>[Cl:1][C:2]1[CH:7]=[CH:6][C:5]([CH:8]([OH:10])[CH3:9])=[CH:4][C:3]=1[S:11]([CH3:14])(=[O:12])=[O:13]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 2

HCID 4311764Sodium borohydrideHCID 581882281-(4-Chloro-3-(methylsulfonyl)phenyl)ethanone

생성물 1

HCID 581879811-(4-Chloro-3-(methylsulfonyl)phenyl)ethanol

시약·촉매·용매 1

HCID 8028Tetrahydrofuran용매

실험 절차

A round bottom flask was charged with 1-(4-chloro-3-(methylsulfonyl)phenyl)ethanone (12.0 g, 50.0 mmol) and tetrahydrofuran (100 mL) at 0° C. Sodium borohydride (3.7 g, 100 mmol) was added in portions and the reaction was stirred for 12 h at room temperature. The reaction was quenched with ice and extracted with MTBE. The organic solvents were removed under reduced pressure and the residue was purified by flash chromatography to get the title compound.

후처리

  1. customThe reaction was quenched with ice
  2. extractionextracted with MTBE
  3. customThe organic solvents were removed under reduced pressure
  4. customthe residue was purified by flash chromatography

출처 및 근거

ORD 기록
ord-04c9c3ac5a06490b9bbfb2cb5b8cfa06
출처 데이터셋
uspto-grants-2015_02
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08946439B2

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