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Ammonium Hydroxide → 2,3-Dichlorobenzenesulfonamide

HRID 236517
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HRID 236517 반응식
[Cl:1][C:2]1[C:7]([Cl:8])=[CH:6][CH:5]=[CH:4][C:3]=1[S:9](Cl)(=[O:11])=[O:10].[OH-].[NH4+:14]>O1CCCC1>[Cl:1][C:2]1[C:7]([Cl:8])=[CH:6][CH:5]=[CH:4][C:3]=1[S:9]([NH2:14])(=[O:11])=[O:10]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 2

HCID 14923Ammonium HydroxideHCID 27342222,3-Dichlorobenzene-1-sulfonyl chloride

생성물 1

HCID 83179472,3-Dichlorobenzenesulfonamide

시약·촉매·용매 1

HCID 8028Tetrahydrofuran용매

실험 절차

To a stirred solution of 60.0 g of 2,3-dichlorobenzenesulfonyl chloride in 500 mL of tetrahydrofuran at 0° C. was added 30 mL of concentrated ammonium hydroxide (30%) dropwise at a rate that maintained the temperature below 15° C. After an additional stirring period of 0.5 hr, the tetrahydrofuran was evaporated under reduced pressure. The resultant solid residue was triturated with 500 mL of water, filtered, and the collected solid washed twice with 100-mL portions of water and dried to yield 52 g of 2,3-dichlorobenzenesulfonamide as a tan solid, m.p. 210°-226° C.; IR (nujol): 3360, 3250, 1370, 1175, 1165 cm-1.

후처리

  1. temperaturemaintained the temperature below 15° C
  2. customthe tetrahydrofuran was evaporated under reduced pressure
  3. customThe resultant solid residue was triturated with 500 mL of water
  4. filtrationfiltered
  5. washthe collected solid washed twice with 100-mL portions of water
  6. customdried

출처 및 근거

ORD 기록
ord-e038212b29fc4d82b0b4d1d85de1e186
출처 데이터셋
uspto-grants-1987_02
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US04645527

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