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llms.txt · MCP 가이드개인정보처리방침 · 이용약관 · 지원v1.8.0
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Dichloromethane → 2-Bromophenylmethylsulfoxide

HRID 1420839
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HRID 1420839 반응식
[OH:1]OS([O-])=O.[K+].[Br:7][C:8]1[CH:13]=[CH:12][CH:11]=[CH:10][C:9]=1[S:14][CH3:15].C(=O)(O)[O-].[Na+].ClCCl>O.CC(C)=O>[Br:7][C:8]1[CH:13]=[CH:12][CH:11]=[CH:10][C:9]=1[S:14]([CH3:15])=[O:1]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

7

반응물 4

HCID 6344DichloromethaneHCID 881662-BromothioanisoleHCID 516892Sodium BicarbonateHCID 23707502Potassium hydroxy sulfite

생성물 1

HCID 110748732-Bromophenylmethylsulfoxide수율 113.2%

시약·촉매·용매 2

HCID 180Acetone용매HCID 962Water용매2회

실험 절차

Oxone (9.7 g) in water (40 ml) was added slowly to a stirred, cooled cooled (0° C.) solution of 2-bromothioanisole (5 g, 24.6 mmol) and sodium bicarbonate (16 g) in acetone (20 ml). The mixture was stirred for at room temperature 16 h., then water and dichloromethane was added. The layers were separated and the organic phase was dried (MgSO4) and the solvent was evaporated under reduced pressure. The residue was purified by chromatography on silica gel, eluting with hexane/EtOAc (80:20 increasing to 40:60) to give the title compound (6.1 g). m/z (ES+) 219 (M+1).

후처리

  1. temperaturecooled
  2. customThe layers were separated
  3. dry with materialthe organic phase was dried (MgSO4)
  4. customthe solvent was evaporated under reduced pressure
  5. customThe residue was purified by chromatography on silica gel
  6. washeluting with hexane/EtOAc (80:20 increasing to 40:60)

출처 및 근거

ORD 기록
ord-05da3fab12bc48b6b6030ec94b6d3426
출처 데이터셋
uspto-grants-2000_06
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US06071927

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