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Thionyl Chloride → 4-(Benzyloxy)benzene-1-sulfonyl chloride

HRID 643987
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HRID 643987 반응식
S(Cl)([Cl:3])=O.[Na+].[CH2:6]([O:13][C:14]1[CH:19]=[CH:18][C:17]([S:20]([O-:23])(=O)=[O:21])=[CH:16][CH:15]=1)[C:7]1[CH:12]=[CH:11][CH:10]=[CH:9][CH:8]=1>CN(C=O)C>[CH2:6]([O:13][C:14]1[CH:19]=[CH:18][C:17]([S:20]([Cl:3])(=[O:23])=[O:21])=[CH:16][CH:15]=1)[C:7]1[CH:12]=[CH:11][CH:10]=[CH:9][CH:8]=1
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 2

HCID 24386Thionyl ChlorideHCID 23685655Sodium p-benzyloxybenzenesulfonate

생성물 1

HCID 47383854-(Benzyloxy)benzene-1-sulfonyl chloride

시약·촉매·용매 1

HCID 6228Dimethylformamide촉매

실험 절차

Thionyl chloride (200 mL, 326.2 grams, 2742 mmol) is added to the solid title A compound, 4-benzyloxybenzenesulfonic acid sodium salt, followed by 10 drops of DMF. The mixture is heated to reflux overnight and then concentrated under vacuum. Hot toluene (250 mL) is added, and the mixture is filtered. The filtrate is concentrated under vacuum. Toluene is again added to the residue followed by filtration and concentration under vacuum to give 4-benzyloxybenzenesulfonyl chloride as a white solid.

후처리

  1. temperatureThe mixture is heated
  2. temperatureto reflux overnight
  3. concentrationconcentrated under vacuum
  4. additionHot toluene (250 mL) is added
  5. filtrationthe mixture is filtered
  6. concentrationThe filtrate is concentrated under vacuum
  7. additionToluene is again added to the residue
  8. filtrationfollowed by filtration and concentration under vacuum

출처 및 근거

ORD 기록
ord-93e94bfbd5a040bf9a50fc7449853313
출처 데이터셋
uspto-grants-2010_04
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US07700637B2

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