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HRID 41699作成日:2026年10月25日

Ammonia → Methyl 4-aminoadamantane-1-carboxylate

https://huagongshe.com/reaction/41699

反応式

関与物質

役割名称HCID仕込み量
反応物AmmoniaHCID 222—
反応物Methyl 4-oxoadamantane-1-carboxylateHCID 4078246—
反応物Sodium borohydrideHCID 4311764—
溶媒MethanolHCID 887—
生成物Methyl 4-aminoadamantane-1-carboxylateHCID 57425932—

反応手順

5 g of 4-oxoadamantane-1-carboxylic acid methyl ester are placed in 26 ml of methanol under nitrogen. 86 ml of a 7N solution of ammonia in methanol are added. The reaction medium is stirred for 18 h, 4 g of sodium borohydride are then added at 0° C. and the reaction medium is stirred for a further 3 h. After concentrating to dryness under reduced pressure and adding water and ethyl acetate, the aqueous phase is extracted three times in ethyl acetate. The organic phases are combined, dried over magnesium sulphate and concentrated to dryness. The crude product obtained is chromatographed on silica gel, elution being carried out with a gradient of heptane/acetone/methanol/NH4OH solvent from 1/0/0 to 4/5/1/0.1. 1.5 g of 4-aminoadamantane-1-carboxylic acid methyl ester are obtained in the form of a mixture of cis/trans (1/3) isomers.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08530657B2
出典データセットuspto-grants-2013_09
ORD IDord-f529236978c34c48bab4f27e15756ed0
出典メモuspto-grants-2013_09