Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 586132Generated: October 25, 2026

Ammonia → tert-butyl N-(1-carbamoylcyclopropyl)carbamate

https://huagongshe.com/reaction/586132

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAmmoniaHCID 222—
ReactantTetrahydrofuranHCID 8028—
ReactantTriethylamineHCID 8471—
ReactantEthyl chloroformateHCID 10928—
Reactant1-Amino-2-(tert-butoxycarbonyl)cyclopropane-1-carboxylic acidHCID 20041317—
Solvent1,4-DioxaneHCID 31275—
Producttert-butyl N-(1-carbamoylcyclopropyl)carbamateHCID 2082555472.5%

Reaction Steps

To a stirred solution of Boc-1-aminocyclopropane-1-carboxylic acid (25 g, 124 mmol) and triethylamine (19 mL, 1.1 equivalent) in THF (200 mL) at −10° C. ethylchloroformate (13 mL, 1.1 equivalent) was added slowly. The mixture was stirred at this temperature for 20 min before a solution of ammonia in 1,4-dioxane (0.5 M, 300 mL) was added. It was allowed to warm to room temperature and stirred overnight. It was concentrated, diluted with water, extracted with dichloromethane, washed with brine, dried (sodium sulfate), concentrated again and dried to give (1-carbamoyl-cyclopropyl)-carbamic acid tert-butyl ester (18 g, 72.5%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06936606B2
Source datasetuspto-grants-2005_08
ORD IDord-3132e197b0da4a7cb748d034b2b5fbb0
Source noteuspto-grants-2005_08