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Sodium borohydride → 2-Amino-5-(1-hydroxyethyl)benzenesulfonamide

HRID 496101
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HRID 496101 반응식
[C:1]([C:4]1[CH:5]=[CH:6][C:7]([NH2:14])=[C:8]([S:10]([NH2:13])(=[O:12])=[O:11])[CH:9]=1)(=[O:3])[CH3:2].[BH4-].[Na+]>CCO>[NH2:14][C:7]1[CH:6]=[CH:5][C:4]([CH:1]([OH:3])[CH3:2])=[CH:9][C:8]=1[S:10]([NH2:13])(=[O:11])=[O:12]
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참가 물질

4

반응물 2

HCID 4311764Sodium borohydrideHCID 129523995-Acetyl-2-aminobenzenesulfonamide2회

생성물 1

HCID 223240092-Amino-5-(1-hydroxyethyl)benzenesulfonamide수율 37%

시약·촉매·용매 1

HCID 702Ethanol용매

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온도
25 °C

실험 절차

5-Acetyl-2-aminobenzenesulfonamide (see compound 13) (0.95 g, 4.4 mmol) was suspended in 96% o EtOH (50 ml) and NaBH4 (0.46 g, 12 mmol) was added in one portion. The mixture was stirred at 25° C. for 4 h and filtered through Celite and the solvent was removed under reduced pressure. The residue was treated with sat. NaHCO3 (50 ml) and extracted with EtOAc (2×50 ml), dried (Na2SO4) and evaporated to dryness. Flash-chromatography with EtOAc:n-hexane:Et3N (200:100:4, v/v/v) as eluent gave 0.35 g (37%) of 2-amino-5-(1-hydroxyethyl)benzenesulfonamide as light-brown powder. M.p. 160-162° C.

후처리

  1. additionwas added in one portion
  2. filtrationfiltered through Celite
  3. customthe solvent was removed under reduced pressure
  4. additionThe residue was treated with sat. NaHCO3 (50 ml)
  5. extractionextracted with EtOAc (2×50 ml)
  6. dry with materialdried (Na2SO4)
  7. customevaporated to dryness

출처 및 근거

ORD 기록
ord-c47a93b3a62f4ca0b6bcb01c860988f8
출처 데이터셋
uspto-grants-2005_09
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US06943159B1

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