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llms.txt · MCP 가이드개인정보처리방침 · 이용약관 · 지원v1.8.0
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Dimethylamine → 4-fluoro-N,N-dimethylbenzenesulfonamide

HRID 371476
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HRID 371476 반응식
[F:1][C:2]1[CH:7]=[CH:6][C:5]([S:8](Cl)(=[O:10])=[O:9])=[CH:4][CH:3]=1.[CH3:12][NH:13][CH3:14]>C(Cl)Cl>[F:1][C:2]1[CH:7]=[CH:6][C:5]([S:8]([N:13]([CH3:14])[CH3:12])(=[O:10])=[O:9])=[CH:4][CH:3]=1
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참가 물질

4

반응물 2

HCID 674DimethylamineHCID 95884-Fluorobenzenesulfonyl chloride

생성물 1

HCID 7993014-fluoro-N,N-dimethylbenzenesulfonamide

시약·촉매·용매 1

HCID 6344Dichloromethane용매

실험 절차

A solution of 38.9 g (0.20 mole) of 4-fluorobenzenesulfonylchloride in 20 ml of methylene chloride was added slowly to 300 ml of a 40% aqueous dimethylamine solution during 0.5 hour period. The reaction was exothermic. After the reaction mixture was cooled a yellow solid was precipitated. The solid was collected, dissolved in 300 ml of ethyl acetate, and dried over magnesium sulfate. The solution was concentrated to 100 ml and a light yellow crystal formed. The crystal was collected and air-dried to afford 39 g of the product, mp 40°-43° C.

후처리

  1. temperatureAfter the reaction mixture was cooled a yellow solid
  2. customwas precipitated
  3. customThe solid was collected
  4. dissolutiondissolved in 300 ml of ethyl acetate
  5. dry with materialdried over magnesium sulfate
  6. concentrationThe solution was concentrated to 100 ml
  7. customa light yellow crystal formed
  8. customThe crystal was collected
  9. customair-dried

출처 및 근거

ORD 기록
ord-50892e292b354823bf6126a20a71ccd5
출처 데이터셋
uspto-grants-1985_07
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US04532240

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