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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2176875Generated: October 31, 2026

Ammonia → HCID 178453949, compound

https://huagongshe.com/reaction/2176875

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAmmoniaHCID 222—
ReactantPivaloyl chlorideHCID 62493—
ReactantHCID 178453971HCID 178453971—
SolventChloroformHCID 6212—
SolventTriethylamineHCID 8471—
ProductHCID 178453949HCID 17845394991.8%

Reaction Steps

Pivaloyl chloride (0.36 ml, 2.96 mmol) was added to a solution of cis-4-[[(1,1-dimethylethoxy)carbonyl]amino]-cyclohexanecarboxylic acid (600 mg, 2.47 mmol) in CHCl3 (10 ml), triethylamine (0.7 ml) at 0° C. and stirred for 1 h. Then aqueous ammonia was added to the reaction mixture and stirred for 1 h. After completion of reaction, the reaction mixture was diluted with CHCl3 (2×25 ml). The organic layer was washed with saturated sodium bicarbonate solution, brine and dried over anhydrous sodium sulfate. The organic layer was concentrated under vacuum, the crude compound was washed with hexane (2×6 ml) and dried to afford 500 mg (91.8%) of cis-tert-butyl-4-carbamoylcyclohexylcarbamate as white color solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09067888B2
Source datasetuspto-grants-2015_06
ORD IDord-424842985bf1472b85735d687d338a2e
Source noteuspto-grants-2015_06