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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1438994Generated: November 2, 2026

Triethylamine → HCID 54032578, compound

https://huagongshe.com/reaction/1438994

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
ReactantEthyl chloroformateHCID 10928—
ReactantN-[(Cyclohexylmethoxy)carbonyl]-L-tyrosineHCID 54310629—
SolventTetrahydrofuranHCID 8028—
ProductHCID 54032578HCID 54032578—

Reaction Steps

In 30 ml of tetrahydrofuran, 3.2 g of N-(cyclohexylmethoxycarbonyl)-tyrosine was dissolved. To the solution were added 1.1 g of ethyl chlorocarbonate and 1.0 g of triethylamine while cooling with ice and stirring. After stirring the mixture for 10 minutes, the precipitate was removed by filtration. The filtrate was added to a suspension of 1.0 g of sodium borohydride and 10 ml of tetrahydrofuran cooled with ice. The mixture was stirred for 2 hours, then neutralized with hydrochloric acid and concentrated in vacuo. The residue was extracted with ethyl acetate and the extract was washed with water, dried and concentrated to dryness. The residue was crystallized from ethyl acetate-petroleum ether to give 2.3 of N-(cyclohexylmethoxycarbonyl)-tyrosinol with a melting point of 121-126° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04057629
Source datasetuspto-grants-1977_11
ORD IDord-09ed967d20cb4a399c7bc7ff57724039
Source noteuspto-grants-1977_11