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Thionyl Chloride → 2-Benzyloxy-ethanesulfonyl chloride

HRID 2078638
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HRID 2078638 반응식
[CH2:1]([O:8][CH2:9][CH2:10][S:11]([OH:14])(=O)=[O:12])[C:2]1[CH:7]=[CH:6][CH:5]=[CH:4][CH:3]=1.S(Cl)([Cl:17])=O>CN(C)C=O>[CH2:1]([O:8][CH2:9][CH2:10][S:11]([Cl:17])(=[O:14])=[O:12])[C:2]1[CH:7]=[CH:6][CH:5]=[CH:4][CH:3]=1
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참가 물질

4

반응물 2

HCID 24386Thionyl ChlorideHCID 23171545HCID 23171545, 화합물

생성물 1

HCID 641796232-Benzyloxy-ethanesulfonyl chloride

시약·촉매·용매 1

HCID 6228Dimethylformamide용매

실험 절차

To a 2-(benzyloxy)ethanesulfonic acid (4.0 g) was added thionyl chloride (13.5 ml) dropwise at ambient temperature for 15 minutes and the mixture was stirred at the same temperature for 10 minutes. To the mixture was added dropwise N,N-dimethylformamide (0.072 ml) at ambient temperature. The mixture was stirred at the same temperature for 20 minutes and refluxed for 1 hour. After cooling down to room temperature, the mixture was evaporated under reduced pressure to give 2-(benzyloxy)ethanesulfonyl chloride (4.1 g).

후처리

  1. stirringThe mixture was stirred at the same temperature for 20 minutes
  2. temperaturerefluxed for 1 hour
  3. customthe mixture was evaporated under reduced pressure

출처 및 근거

ORD 기록
ord-8da05fb1ee3346c88a79edd938e9d889
출처 데이터셋
uspto-grants-2011_04
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US07928264B2

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