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Pyridine → 1-Acetoxy-5-chloro-2-methylsulfonylindane

HRID 2084731
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반응식

HRID 2084731 반응식
[Cl:1][C:2]1[CH:3]=[C:4]2[C:8](=[CH:9][CH:10]=1)[CH:7]([OH:11])[CH:6]([S:12]([CH3:15])(=[O:14])=[O:13])[CH2:5]2.N1C=CC=CC=1.[C:22](OC(=O)C)(=[O:24])[CH3:23]>ClCCl>[C:22]([O:11][CH:7]1[C:8]2[C:4](=[CH:3][C:2]([Cl:1])=[CH:10][CH:9]=2)[CH2:5][CH:6]1[S:12]([CH3:15])(=[O:14])=[O:13])(=[O:24])[CH3:23]
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참가 물질

5

반응물 3

HCID 1049PyridineHCID 7918Acetic AnhydrideHCID 98347545-Chloro-2-methylsulfonylindan-1-ol

생성물 1

HCID 99438231-Acetoxy-5-chloro-2-methylsulfonylindane

시약·촉매·용매 1

HCID 6344Dichloromethane용매

실험 절차

0.247 g (1 mmol) of 5-chloro-2-methylsulfonylindan-1-ol is dissolved in 5 ml of dichloromethane. 1 ml of pyridine and 1 ml of acetic anhydride are added to the solution, and the reaction mixture is then stirred at room temperature for 2 days. The reaction solution is evaporated completely and the residue is taken up in dichloromethane and extracted with dilute citric acid. The organic phase is separated off, concentrated and purified chromatographically (silica gel; dichloromethane/methanol 20/1). This gives 1-acetoxy-5-chloro-2-methylsulfonylindane of melting point 136° C.

후처리

  1. customThe reaction solution is evaporated completely
  2. extractionextracted with dilute citric acid
  3. customThe organic phase is separated off
  4. concentrationconcentrated
  5. custompurified chromatographically (silica gel; dichloromethane/methanol 20/1)

출처 및 근거

ORD 기록
ord-c44c60862176409b930be4ea56700993
출처 데이터셋
uspto-grants-2004_04
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US06717008B2

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