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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1031748Generated: October 25, 2026

Hydrochloric Acid → HCID 178485750, compound

https://huagongshe.com/reaction/1031748

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantDimethylformamideHCID 6228—
ReactantTriethylamineHCID 8471—
ReactantEthyl chloroformateHCID 10928—
ReactantHCID 178453624HCID 178453624—
SolventTetrahydrofuranHCID 8028—
ProductHCID 178485750HCID 178485750—

Reaction Steps

On the other hand, trans-4-(t-butoxycarbonylaminomethyl)cyclohexyl carboxylic acid (203 g) was dissolved in dry tetrahydrofuran (80 ml) and triethylamine (1.19 ml) was added under ice-cooling to the solution, and the solution was stirred for 10 minutes. Subsequently, a solution of ethyl chlorocarbonate (0.85 g) in dry tetrahydrofuran (5 ml) was added and the mixture was further stirred for 20 minutes. The mixture was added to a mixture of the hydrochloride (II) previously obtained, triethylamine (1.19 ml), and N,N-dimethylformamide (5 ml) under ice-cooling, followed by stirring for 2 hours and again under room temperature for 2 hours. The solvent was evaporated under a reduced pressure, the residue was diluted with ice-water, and the precipitates were collected by filtration and washed with water. The product was washed with 10% aqueous citric acid and with water, followed by washing with 50% aqueous ethyl alcohol, 50% ethyl alcohol-ethyl ether, and dried to give N-[trans-4-(t-butoxycarbonylaminomethyl)cyclohexylcarbonyl]-L-phenylalanine methylamide (III) (2.57 g).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04954512
Source datasetuspto-grants-1990_09
ORD IDord-aed487cfb7e14ef8aff62a12f89f5f3f
Source noteuspto-grants-1990_09