反応式
C([O:3][C:4]([CH:6]1[CH2:11][CH2:10][N:9]([CH3:12])[CH2:8][CH2:7]1)=[O:5])C.[ClH:13]>>[ClH:13].[CH3:12][N:9]1[CH2:10][CH2:11][CH:6]([C:4]([OH:5])=[O:3])[CH2:7][CH2:8]1参加物
3
実験手順
A solution of 1-methyl-piperidine-4-carboxylic acid ethyl ester (2.0 g, 11.7 mmol) in conc. hydrochloric acid (20 mL) was heated to 100° C. and maintained for 6 h. The mixture was then concentrated to dryness in vacuo to give a solid, which was washed with acetonitrile-diethyl ether (1:1) and dried in vacuo to afford 1-methyl-piperidine-4-carboxylic acid hydrochloride (1.0 g, 48%) as an off-white solid.
後処理
- temperaturemaintained for 6 h
- concentrationThe mixture was then concentrated to dryness in vacuo
- customto give a solid, which
- washwas washed with acetonitrile-diethyl ether (1:1)
- customdried in vacuo
出典と根拠
- ORDレコード
- ord-b2d4f887d1504bc6ae79c363e192ce23
- 出典データセット
- uspto-grants-2013_09
- 特許番号
- US08524705B2
関連ノート
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