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Benzenesulfinic acid → 2-(Benzenesulfonyl)-5-methoxyoxolane

HRID 22481
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반응식

HRID 22481 반응식
[CH3:1][O:2][CH:3]1[CH2:7][CH2:6][CH:5](OC)[O:4]1.[C:10]1([S:16]([OH:18])=[O:17])[CH:15]=[CH:14][CH:13]=[CH:12][CH:11]=1.[Cl-].[Ca+2].[Cl-]>C(Cl)Cl>[C:10]1([S:16]([CH:5]2[CH2:6][CH2:7][CH:3]([O:2][CH3:1])[O:4]2)(=[O:18])=[O:17])[CH:15]=[CH:14][CH:13]=[CH:12][CH:11]=1
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

5

반응물 3

HCID 12057Benzenesulfinic acidHCID 790982,5-DimethoxytetrahydrofuranHCID 5284359Calcium Chloride

생성물 1

HCID 199304622-(Benzenesulfonyl)-5-methoxyoxolane수율 55%

시약·촉매·용매 1

HCID 6344Dichloromethane용매

실험 절차

2,5-Dimethoxytetrahydrofuran (17.1 ml, 0.13M) was added dropwise to a stirred solution of benzenesulphinic acid (17.0 g, 0.12M) in dry DCM (100 ml) containing a suspension of powdered calcium chloride (1.0 g) at room temperature under argon. After 4 h, the solution was washed with water (2×50 ml), dried over anhydrous sodium sulphate, filtered and evaporated. The product was crystalised (diethyl ether/hexane) to give 2-benzenesulphonyl-5-methoxytetrahydro-furan as a white crystalline solid (15.9 g, 55%).

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후처리

  1. additioncontaining
  2. washthe solution was washed with water (2×50 ml)
  3. dry with materialdried over anhydrous sodium sulphate
  4. filtrationfiltered
  5. customevaporated
  6. customThe product was crystalised (diethyl ether/hexane)

출처 및 근거

ORD 기록
ord-b6ed6f7d4f744f7289f901854ca27289
출처 데이터셋
uspto-grants-1995_06
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US05428168

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