1-Aminocyclohexanecarboxylic acid → 1-[(Methoxycarbonyl)amino]cyclohexanecarboxylic acid
反応式
[NH2:1][C:2]1([C:8]([OH:10])=[O:9])[CH2:7][CH2:6][CH2:5][CH2:4][CH2:3]1.Cl[C:12]([O:14][CH3:15])=[O:13].[OH-].[Na+]>C1COCC1.O>[CH3:15][O:14][C:12]([NH:1][C:2]1([C:8]([OH:10])=[O:9])[CH2:7][CH2:6][CH2:5][CH2:4][CH2:3]1)=[O:13]参加物
実験手順
A suspension of 39.9 g (279 mmol) of 1-aminocyclohexane-1-carboxylic acid in a mixture of 75 ml of THF and 75 ml of water was treated dropwise with 23.8 ml of methyl chloroformate, dissolved in 40 ml of THF, such that the temperature of the suspension did not rise above 50° C. In the course of this, the pH of the solution was kept between 8.5 and 9.5 by addition of 25% strength sodium hydroxide solution. After stirring at pH 8 for 30 minutes, the mixture was diluted with water, the THF was removed in vacuo and the aqueous phase was washed twice with methyl tert-butyl ether. The aqueous phase was adjusted to pH 2 using 6 N hydrochloric acid and extracted successively with methyl tert-butyl ether and dichloromethane. The combined organic phases were concentrated in vacuo. The residue was triturated with diethyl ether and the product was filtered off. 47.85 g (85%) of 1-methoxycarbonylaminocyclohexane-1-carboxylic acid were obtained.
後処理
- customdid not rise above 50° C
- customthe THF was removed in vacuo
- washthe aqueous phase was washed twice with methyl tert-butyl ether
- extractionextracted successively with methyl tert-butyl ether and dichloromethane
- concentrationThe combined organic phases were concentrated in vacuo
- customThe residue was triturated with diethyl ether
- filtrationthe product was filtered off
出典と根拠
- ORDレコード
- ord-eef5f187c73e47fea5a85b16005185fc
- 出典データセット
- uspto-grants-2002_06
- 特許番号
- US06399643B1
反応ノート
読み込み中…