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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1510040Generated: October 26, 2026

Ammonia → Methyl 4-aminoadamantane-1-carboxylate

https://huagongshe.com/reaction/1510040

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 numberUS08211892B2
Source datasetuspto-grants-2012_07
ORD IDord-59f7643fbfdd47f4be972d74ce049dc3
Source noteuspto-grants-2012_07