Dimethyl Sulfate → Methyl 2-chloronicotinate

HRID 274855

反応式

HRID 274855 の反応式
[Cl:1][C:2]1[C:7]([C:8]([OH:10])=[O:9])=[CH:6][CH:5]=[CH:4][N:3]=1.S(OC)(O[CH3:15])(=O)=O.C(=O)([O-])[O-].[K+].[K+]>CC(C)=O>[Cl:1][C:2]1[C:7]([C:8]([O:10][CH3:15])=[O:9])=[CH:6][CH:5]=[CH:4][N:3]=1

参加物

5

実験手順

2-Chloro-3-pyridinecarboxylic acid, methyl ester (11) is prepared as follows: a suspension of 22.06 g (140 mmol) of 2-chloro-3-pyridinecarboxylic acid (10), 14.6 mL (154 mmol) of dimethyl sulfate, 29 g (210 mmol) of anhydrous powdered potassium carbonate, and 140 mL of acetone is stirred at room temperature overnight. The mixture is filtered, the salts are washed with acetone, and the filtrate is concentrated to an oil that is diluted with dichloromethane. The organic phase is washed with saturated aqueous sodium dicarbonate, dried, then filtered through a pad of silica gel (230-400 mesh). The filtrate is concentrated to give an oil that is distilled at 90°-91° C./0.17 mm to leave 19.9 g of the pure product as a colorless oil.

後処理

  1. filtrationThe mixture is filtered
  2. washthe salts are washed with acetone
  3. concentrationthe filtrate is concentrated to an oil that
  4. additionis diluted with dichloromethane
  5. washThe organic phase is washed with saturated aqueous sodium dicarbonate
  6. customdried
  7. filtrationfiltered through a pad of silica gel (230-400 mesh)
  8. concentrationThe filtrate is concentrated
  9. customto give an oil that
  10. distillationis distilled at 90°-91° C./0.17 mm

出典と根拠

ORDレコード
ord-9717230ce4f84669bd43a6766fd0b8e9
出典データセット
uspto-grants-1995_02
特許番号
US05391554

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