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

HRID 496101
ノート
印刷プレビュー

反応式

HRID 496101 の反応式
[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]
参加物反応条件実験手順後処理出典と根拠反応ノート

参加物

4

反応物 2

HCID 4311764Sodium borohydrideHCID 129523995-Acetyl-2-aminobenzenesulfonamide2 回

生成物 1

HCID 223240092-Amino-5-(1-hydroxyethyl)benzenesulfonamide収率 37%

試薬・触媒・溶媒 1

HCID 702Ethanol溶媒

反応条件

温度
25 °C

実験手順

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.

後処理

  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

出典と根拠

ORDレコード
ord-c47a93b3a62f4ca0b6bcb01c860988f8
出典データセット
uspto-grants-2005_09
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US06943159B1

反応ノート

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