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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1662038Generated: October 30, 2026

methyl (1S,2R)-2-[(tert-butoxycarbonyl)amino]cyclopentanecarboxylate → methyl (1S,2R)-2-aminocyclopentane-1-carboxylate hydrochloride

https://huagongshe.com/reaction/1662038

Reaction equation

Participants

RoleNameHCIDCharge
Reactantmethyl (1S,2R)-2-[(tert-butoxycarbonyl)amino]cyclopentanecarboxylateHCID 11322482—
ReactantHydrogen chloride-ethyl acetateHCID 21866389—
SolventEthyl AcetateHCID 8857—
Productmethyl (1S,2R)-2-aminocyclopentane-1-carboxylate hydrochlorideHCID 14698816—

Reaction Steps

To a mixture of methyl (1S,2R)-2-[(tert-butoxycarbonyl)amino]cyclopentanecarboxylate (0.84 g) and ethyl acetate (2.5 ml) was added a 4 M hydrogen chloride/ethyl acetate solution (5.0 ml) under ice-cooling, followed by stirring at room temperature for 2.5 hours. The reaction mixture was concentrated under reduced pressure to obtain methyl (1S,2R)-2-aminocyclopentanecarboxylate hydrochloride (0.72 g).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08030489B2
Source datasetuspto-grants-2011_10
ORD IDord-0f6e303c9e86432cbf16bfaff76d4751
Source noteuspto-grants-2011_10