Sodium hydride → 5-(t-Butoxycarbonylmethyl)oxy-2-hydroxymethylpyridine

HRID 1940382ノート

反応式

HRID 1940382 の反応式
[OH:1][C:2]1[CH:3]=[CH:4][C:5]([CH2:8][OH:9])=[N:6][CH:7]=1.[H-].[Na+].Br[CH2:13][C:14]([O:16][C:17]([CH3:20])([CH3:19])[CH3:18])=[O:15]>CN(C=O)C.C(OCC)(=O)C>[C:17]([O:16][C:14]([CH2:13][O:1][C:2]1[CH:3]=[CH:4][C:5]([CH2:8][OH:9])=[N:6][CH:7]=1)=[O:15])([CH3:20])([CH3:19])[CH3:18]

参加物

6

実験手順

The solution of 5-hydroxy-2-hydroxymethylpyridine (5.0 g) in DMF (10 ml) was titrated under ice-cooling in the suspension of sodium hydride (60% purity, 1.6 g) in DMF (10 ml). After 10 minutes, the mixture was heated to room temperature and stirred for 15 minutes. After t-butyl bromoacetate (6 ml) was added to the mixture under ice-cooling, the resulting mixture was stirred under ice-cooling for 10 minutes and at room temperature for 45 minutes. The reaction mixture was diluted with ethyl acetate, washed with water and brine and dried over anhydrous magnesium sulfate. After the solvents were removed by distillation, the residue was purified by column chromatography on silica gel with an eluent system of chloroform→chloroform:methanol=50:1 to give 8.16 g of 5-(t-butoxycarbonylmethyl)oxy-2-hydroxymethylpyridine (yield, 85%).

後処理

  1. temperaturecooling
  2. stirringthe resulting mixture was stirred under ice-
  3. temperaturecooling for 10 minutes and at room temperature for 45 minutes
  4. washwashed with water and brine
  5. dry with materialdried over anhydrous magnesium sulfate
  6. customAfter the solvents were removed by distillation
  7. customthe residue was purified by column chromatography on silica gel with an eluent system of chloroform→chloroform

出典と根拠

ORDレコード
ord-0e7f45ad76aa42c3b5ebd1d5d8f5dd2e
出典データセット
uspto-grants-1997_12
特許番号
US05698692

反応ノート

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