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Ammonium Hydroxide → 3,5-Difluorobenzenesulfonamide

HRID 83899
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HRID 83899 반응식
[F:1][C:2]1[CH:3]=[C:4]([S:9](Cl)(=[O:11])=[O:10])[CH:5]=[C:6]([F:8])[CH:7]=1.[NH4+:13].[OH-]>C1COCC1>[F:1][C:2]1[CH:3]=[C:4]([S:9]([NH2:13])(=[O:11])=[O:10])[CH:5]=[C:6]([F:8])[CH:7]=1
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참가 물질

4

반응물 2

HCID 14923Ammonium HydroxideHCID 27740583,5-Difluorobenzenesulfonyl chloride

생성물 1

HCID 4462753,5-Difluorobenzenesulfonamide수율 88%

시약·촉매·용매 1

HCID 8028Tetrahydrofuran용매

실험 절차

To a solution of 3,5-difluorobenzenesulfonyl chloride (25 g, 0.117 mol) in THF (150 mL) was added 35% aq. NH4OH (120 mL) over 1 h in an ice-bath. After the reaction was complete, it was evaporated in vacuo. To a solution of this residue in water (150 mL) was added 2N HCl (1 mL). After stirring 1 h, the reaction mixture was filtered and dried under high vacuum to give 3,5-difluorobenzenesulfonamide as a light brown solid (19.9 g, 88%). 1H NMR (400 MHz, CDCl3) δ 7.49-7.44 (m, 2H), 7.04-6.99 (m, 2H).

후처리

  1. customit was evaporated in vacuo
  2. additionTo a solution of this residue in water (150 mL) was added 2N HCl (1 mL)
  3. filtrationthe reaction mixture was filtered
  4. customdried under high vacuum

출처 및 근거

ORD 기록
ord-41a2ed1b02ef47148905575ab7720070
출처 데이터셋
uspto-grants-2014_09
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08846739B2

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