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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1593989Generated: October 30, 2026

Sodium Carbonate → (2-Acetyl-cyclohexyl)-carbamic acid benzyl ester

https://huagongshe.com/reaction/1593989

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium CarbonateHCID 10340—
ReactantBenzyl chloroformateHCID 10387—
ReactantEthyl (1R,2S)-2-aminocyclohexane-1-carboxylate hydrobromideHCID 122236269—
SolventDichloromethaneHCID 6344—
Product(2-Acetyl-cyclohexyl)-carbamic acid benzyl esterHCID 2073258098%

Reaction Steps

To a 0° C. solution of ethyl cis-2-amino-1-cyclohexanecarboxylate HBr salt (22.34 g, 88.6 mmol) in 250 mL of methylene chloride, was added benzyl chloroformate (12.6 mL, 88.3 mmol) and 250 mL of an aqueous sodium carbonate solution. The reaction mixture was stirred for 24 h at ambient temperature. The organic layer was separated and washed with 250 mL of water, dried over sodium sulfate, filtered and concentrated to give a crude liquid. The product was purified by column chromatography (10-50:90-50 ethyl acetate/hexanes) to give 26.45 g of (2-acetyl-cyclohexyl)-carbamic acid benzyl ester as a clear liquid. Yield: 98%, MS: 306 (M+H+).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07300934B2
Source datasetuspto-grants-2007_11
ORD IDord-2ff250ba1c11443fb3c0cf81a0f0bb1e
Source noteuspto-grants-2007_11