反応式
[C:1]([N:4]1[CH2:9][CH2:8][CH:7]([CH2:10][CH2:11][C:12]([OH:14])=O)[CH2:6][CH2:5]1)(=[O:3])[CH3:2].S(Cl)([Cl:17])=O>>[C:1]([N:4]1[CH2:9][CH2:8][CH:7]([CH2:10][CH2:11][C:12]([Cl:17])=[O:14])[CH2:6][CH2:5]1)(=[O:3])[CH3:2]参加物
3
実験手順
To 100 ml of thionyl chloride was added 26 g of 3-(1-acetylpiperidin-4-yl)propionic acid, obtained in Reference Example 1-(2), in small portions with ice-cooling. The mixture was stirred for 5 minutes, after which the excess thionyl chloride was distilled off and the solid residue was washed with diethyl ether to give 26.4 g of 3-(1-acetylpiperidin-4-yl)propionyl chloride as a pale yellow powder.
後処理
- temperaturein small portions with ice-cooling
- distillationafter which the excess thionyl chloride was distilled off
- washthe solid residue was washed with diethyl ether
出典と根拠
- ORDレコード
- ord-d878f7c71dea4699bd97b412d55dc53e
- 出典データセット
- uspto-grants-1993_12
- 特許番号
- US05273974
関連ノート
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