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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2163540Generated: November 2, 2026

Dicyclohexylamine → HCID 16049965, compound

https://huagongshe.com/reaction/2163540

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDicyclohexylamineHCID 7582—
ReactantEthyl bromoacetateHCID 7748—
ReactantL-Tyrosine, N-(1,1-dimethylethoxy)carbonyl-HCID 117439—
SolventDimethylformamideHCID 6228—
ProductHCID 16049965HCID 16049965—

Reaction Steps

A mixture of 7 g (0.025 mol) of t-butyloxycarbonyl-L-tyrosine, 4.53 g (0.025 mol) of dicyclohexylamine and 4.18 g (0.025 mol) of ethyl bromoacetate in 40 ml of dimethylformamide is stirred for 15 hours. The precipitate of dicyclohexylamine hydrobromide which has formed is filtered off and washed with ethyl acetate. The combined filtrates are evaporated to dryness under reduced pressure. An oily residue is obtained which is taken up in ethyl acetate and washed twice with a 2N solution of sulphuric acid, once with water, twice with a solution of potassium bicarbonate and, finally, once with water. After desiccation over magnesium sulphate, the solution is evaporated to dryness. An oily residue is obtained which is dissolved in 50 ml of acetic acid containing 1.8 g (0.05 mol) of gaseous hydrochloric acid. The solution is allowed to stand for 30 minutes and then evaporated to dryness under reduced pressure, and the residue is recrystallised several times from a mixture of isopropanol and ether. 5.7 g of the hydrochloride (yield 75%), which melts at 176°, are collected. [α]Dt = + 12.2°.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04134991
Source datasetuspto-grants-1979_01
ORD IDord-995d7f5777014ffcbd1ac5c95e327711
Source noteuspto-grants-1979_01