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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2200373Generated: November 1, 2026

Methanol → Methyl (1S,3R)-3-aminocyclopentane-1-carboxylate

https://huagongshe.com/reaction/2200373

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethanolHCID 887—
ReactantThionyl ChlorideHCID 24386—
Reactant(1R,3S)-3-aminocyclopentane-1-carboxylic acid hydrochlorideHCID 54611811—
ProductMethyl (1S,3R)-3-aminocyclopentane-1-carboxylateHCID 4508912498%

Reaction Steps

To a solution of (1R,3S)-3-aminocyclopentanecarboxylic acid hydrochloride (2.5 g, 15.09 mmol) in dry methanol (10 ml) under N2 at 0° C. was added thionyl chloride (5.51 ml, 75 mmol) dropwise. The reaction mixture was slowly warmed to room temperature and stirred overnight. The reaction was concentrated in vacuo. The resultant residue was washed with anhydrous diethyl ether (3×30 ml) and dried under high vacuum to afford of (1S,3R)-3-aminocyclopentanecarboxylic acid methyl ester (2.65 g 98%) as the hydrochloride salt that was used in a subsequent reaction without purification.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09359367B2
Source datasetuspto-grants-2016_06
ORD IDord-6353dbb7a62d442189c700f6d6bd7b85
Source noteuspto-grants-2016_06