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Methanol → 1-(Bromomethyl)-2-methanesulfonylbenzene

HRID 1290014
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HRID 1290014 반응식
CS[C:3]1[CH:10]=[CH:9][CH:8]=[CH:7][C:4]=1[CH2:5][Br:6].O[O:12][S:13]([O-:15])=O.[K+].[CH3:17]O>O>[CH3:17][S:13]([C:3]1[CH:10]=[CH:9][CH:8]=[CH:7][C:4]=1[CH2:5][Br:6])(=[O:15])=[O:12]
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참가 물질

5

반응물 3

HCID 887MethanolHCID 217935191-(Bromomethyl)-2-(methylsulfanyl)benzeneHCID 23707502Potassium hydroxy sulfite

생성물 1

HCID 189224741-(Bromomethyl)-2-methanesulfonylbenzene

시약·촉매·용매 1

HCID 962Water용매

실험 절차

To a solution of 124 mg (0.57 mmol) of 2-(methylthio)-benzylbromide in 8.0 mL of methanol was added a solution of 702 mg of oxone in 7.0 mL of water. The solution was stirred for 4.5 h, concentrated in vacuo and purified by silica gel flash chromatography, eluting with 10% ethyl acetate/hexane to give 105 mg of the title compound. mass spec 249(M+). NMR (CDCl3): δ 3.25 (s, 3H), 5.07 (s, 2H), 7.50 (m, 1H), 7.60 (m, 2H), 8.05 (d, 1H).

후처리

  1. concentrationconcentrated in vacuo
  2. custompurified by silica gel flash chromatography
  3. washeluting with 10% ethyl acetate/hexane

출처 및 근거

ORD 기록
ord-11363b0229f34597bd9f6f342ba64980
출처 데이터셋
uspto-grants-1998_05
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US05750549

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