1-(4-Methylbenzene-1-sulfonyl)-1H-indole-3-carbaldehyde → (1-tosyl-1H-indol-3-yl)methanol

HRID 41534

反応式

HRID 41534 の反応式
[S:1]([N:11]1[C:19]2[C:14](=[CH:15][CH:16]=[CH:17][CH:18]=2)[C:13]([CH:20]=[O:21])=[CH:12]1)([C:4]1[CH:10]=[CH:9][C:7]([CH3:8])=[CH:6][CH:5]=1)(=[O:3])=[O:2].[BH4-].[Na+]>CO>[S:1]([N:11]1[C:19]2[C:14](=[CH:15][CH:16]=[CH:17][CH:18]=2)[C:13]([CH2:20][OH:21])=[CH:12]1)([C:4]1[CH:5]=[CH:6][C:7]([CH3:8])=[CH:9][CH:10]=1)(=[O:2])=[O:3]

参加物

4

反応物 2

HCID 7358171-(4-Methylbenzene-1-sulfonyl)-1H-indole-3-carbaldehydeHCID 4311764Sodium borohydride

生成物 1

HCID 839263(1-tosyl-1H-indol-3-yl)methanol収率 92.2%

試薬・触媒・溶媒 1

HCID 887Methanol溶媒

実験手順

To a solution of 1-tosyl-1H-indole-3-carbaldehyde (7 g, 23.385 mmol) in MeOH (70 mL), NaBH4 (1.77 g, 46.769 mmol) was added at 0° C. and the mixture was stirred for 10 min. The reaction mixture was allowed to warm to rt and stirring was continued for 18 h. The solvent was removed under reduced pressure at 45° C. and the crude reaction mixture was quenched with saturated aqueous ammonium chloride solution. Ethyl acetate was added and the organic layer was washed with water and brine. The organic layer was dried over anhydrous sodium sulfate. The organic layer was concentrated under reduced pressure to yield a solid (6.5 g, 92%). [1H-NMR (CDCl3, 300 MHz) δ 8.02-7.95 (m, 1H), 7.82-7.75 (m, 2H), 7.65-7.53 (m, 2H), 7.40-7.19 (m, 4H)].

後処理

  1. stirringstirring
  2. waitwas continued for 18 h
  3. customThe solvent was removed under reduced pressure at 45° C.
  4. customthe crude reaction mixture
  5. customwas quenched with saturated aqueous ammonium chloride solution
  6. additionEthyl acetate was added
  7. washthe organic layer was washed with water and brine
  8. dry with materialThe organic layer was dried over anhydrous sodium sulfate
  9. concentrationThe organic layer was concentrated under reduced pressure

出典と根拠

ORDレコード
ord-13947a147af8496a8baa8ac63ebdbe9e
出典データセット
uspto-grants-2013_09
特許番号
US08530648B2

関連ノート

読み込み中…