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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 276249Generated: October 29, 2026

1-Aminocyclohexanecarboxylic acid → 1-(Cbz-amino)cyclohexanecarboxylic acid

https://huagongshe.com/reaction/276249

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1-Aminocyclohexanecarboxylic acidHCID 1366—
ReactantBenzyl chloroformateHCID 10387—
SolventSodium HydroxideHCID 14798—
Product1-(Cbz-amino)cyclohexanecarboxylic acidHCID 1135788689.1%

Reaction Steps

To a solution of l-aminocyclohexane-1-carboxylic acid (10.0 g, 70.0 mmol) in a 1M NaOH solution (100 mL) was added benzyl chloroformate (12.0 ml, 84.0 mmol). The reaction mixture was stirred for 2 h while maintaining pH 9 by addition of a 1M NaOH solution as necessary. The resulting solution was washed with Et2O (2×100 mL), then the aqueous layer was adjusted to pH 0 with a conc. HCl solution and the solution was extracted with EtOAc (3×150 mL). The combined organic layers were dried (MgSO4) and concentrated under reduced pressure to yield 1-(benzyloxycarbonylamino)cyclohexane-1-carboxylic acid (17.3 g, 89%): TLC (25% EtOAc/hex) Rf0.07.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06353006B1
Source datasetuspto-grants-2002_03
ORD IDord-96e8f18f2acb48c4a45d10eda0248a35
Source noteuspto-grants-2002_03