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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1395809Generated: October 30, 2026

4-Methylmorpholine → t-Butoxycarbonylvalyltyrosine methyl ester

https://huagongshe.com/reaction/1395809

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-MethylmorpholineHCID 7972—
ReactantIsobutyl chloroformateHCID 62365—
ReactantMethyl tyrosinate hydrochlorideHCID 76956—
ReactantBoc-L-ValineHCID 83693—
SolventDichloromethaneHCID 6344—
Productt-Butoxycarbonylvalyltyrosine methyl esterHCID 14752398—

Reaction Conditions

Temperature-70 °C

Reaction Steps

21.7 g of t-butoxycarbonylvaline is dissolved in 200 ml of methylene chloride. 22.2 ml of N-methylmorpholine is added to the solution. The solution is cooled to -70° C. 13.1 ml of isobutylchloroformate is then added. The reaction mixture is again cooled to -70° C. 23.2 g of tyrosine methyl ester hydrochloride is added to the reaction mixture. The reaction mixture is allowed to warm to room temperature, and then is stirred for 16 hours. The reaction mixture is extracted three times with 0.5 M potassium bisulfate and once with brine. The methylene chloride solution is dried over anhydrous sodium sulfate, filtered and stripped of solvent. The residue is dissolved in 200 ml of ethyl ether. The ether solution is added to cold rapidly stirring Skellysolve B. The white precipitate is filtered and dried to afford the product t-butoxycarbonylvalyltyrosine methyl ester.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04204991
Source datasetuspto-grants-1980_05
ORD IDord-2273e8eb9ebd41a58e68eaeaf23ea4ac
Source noteuspto-grants-1980_05