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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 41699Generated: October 25, 2026

Ammonia → Methyl 4-aminoadamantane-1-carboxylate

https://huagongshe.com/reaction/41699

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAmmoniaHCID 222—
ReactantMethyl 4-oxoadamantane-1-carboxylateHCID 4078246—
ReactantSodium borohydrideHCID 4311764—
SolventMethanolHCID 887—
ProductMethyl 4-aminoadamantane-1-carboxylateHCID 57425932—

Reaction Steps

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.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08530657B2
Source datasetuspto-grants-2013_09
ORD IDord-f529236978c34c48bab4f27e15756ed0
Source noteuspto-grants-2013_09