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Hydrochloric Acid → 3-Bromo-4-fluorobenzenesulfonamide

HRID 518332
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HRID 518332 반응식
[Br:1][C:2]1[CH:3]=[C:4]([S:9](Cl)(=[O:11])=[O:10])[CH:5]=[CH:6][C:7]=1[F:8].C(Cl)Cl.[OH-].[NH4+:17].Cl>C1COCC1>[Br:1][C:2]1[CH:3]=[C:4]([S:9]([NH2:17])(=[O:11])=[O:10])[CH:5]=[CH:6][C:7]=1[F:8]
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참가 물질

6

반응물 4

HCID 313Hydrochloric AcidHCID 6344DichloromethaneHCID 14923Ammonium HydroxideHCID 218867333-Bromo-4-fluorobenzene-1-sulfonyl chloride

생성물 1

HCID 790405443-Bromo-4-fluorobenzenesulfonamide수율 60%

시약·촉매·용매 1

HCID 8028Tetrahydrofuran용매

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온도
0 °C

실험 절차

A solution of 3-bromo-4-fluorobenzenesulfonyl chloride (1 g, 3.3 mmol, 90% pure) stirred at 0° C. in THF (15 ml) and DCM (5 ml) was treated with aqueous ammonium hydroxide (28%) by dropwise addition over 15 min. After stirring at 0° C. for 210 min, the mixture was acidified (pH=1) by addition of 1 N HCl (aq). After the mixture was concentrated in vacuo to near dryness, it was treated with water (50 ml), sonicated for 3 min and filtered. After the filter cake was washed sequentially with water (50 ml) and hexanes (100 ml), it was dried in vacuo to afford the title compound (503 mg, 60%) as a white solid which was carried forward without purification. LCMS (M−H)−=253.

후처리

  1. concentrationAfter the mixture was concentrated in vacuo
  2. additionwas treated with water (50 ml)
  3. customsonicated for 3 min
  4. filtrationfiltered
  5. washAfter the filter cake was washed sequentially with water (50 ml) and hexanes (100 ml), it
  6. customwas dried in vacuo

출처 및 근거

ORD 기록
ord-90881ee0511b4f7485bb610d8a5d70cd
출처 데이터셋
uspto-grants-2015_08
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US09115114B2

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