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llms.txt · MCP 가이드개인정보처리방침 · 이용약관 · 지원v1.8.0
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4-Toluenesulfonyl chloride → Acetonitrile, 2-(((4-methylphenyl)sulfonyl)oxy)-

HRID 437177
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HRID 437177 반응식
[C:1](#[N:4])[CH2:2][OH:3].[C:5]1([CH3:15])[CH:10]=[CH:9][C:8]([S:11](Cl)(=[O:13])=[O:12])=[CH:7][CH:6]=1.COCCOC.[OH-].[Na+]>O>[C:5]1([CH3:15])[CH:10]=[CH:9][C:8]([S:11]([O:3][CH2:2][C:1]#[N:4])(=[O:13])=[O:12])=[CH:7][CH:6]=1
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참가 물질

6

반응물 4

HCID 73974-Toluenesulfonyl chlorideHCID 7857HydroxyacetonitrileHCID 80711,2-DimethoxyethaneHCID 14798Sodium Hydroxide

생성물 1

HCID 84525Acetonitrile, 2-(((4-methylphenyl)sulfonyl)oxy)-

시약·촉매·용매 1

HCID 962Water용매2회

실험 절차

Method of preparation: 8.1 g (0.1 mole of glycolonitrile (70% aqueous solution) is added to a cooled (15° -20° C.) mixture of 9.5 g (0.05 mole) of p-toluenesulfonyl chloride in 20 ml. of 1,2-dimethoxyethane and 50 ml. distilled water. A solution of 2.1 g (0.05 mole) of NaOH in 50 ml. distilled water is added slowly with stirring at 20°-25° C. over a period of 6.5 hours, maintaining the pH of the reaction mixture at about 8. The insoluble material is filtered off, washed with cold water, and dried at 40° C. under vacuum to yield 6.8 g (64% conversion) of the product, a light brown solid, m.p. 48°-50.5° C.

후처리

  1. customMethod of preparation
  2. temperaturea cooled
  3. temperaturemaintaining the pH of the reaction mixture at about 8
  4. filtrationThe insoluble material is filtered off
  5. washwashed with cold water
  6. customdried at 40° C. under vacuum
  7. customto yield 6.8 g (64% conversion) of the product

출처 및 근거

ORD 기록
ord-d7f52cd9c8264487915d7e6f4520eb50
출처 데이터셋
uspto-grants-1977_06
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US04029809

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