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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 27347Generated: October 26, 2026

4-Methylmorpholine → carbobenzoxy-beta-alanyl-L-proline t-butyl ester

https://huagongshe.com/reaction/27347

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-MethylmorpholineHCID 7972—
ReactantIsobutyl chloroformateHCID 62365—
ReactantN-Benzyloxycarbonyl-beta-alanineHCID 75313—
Reactanttert-Butyl L-prolinate hydrochlorideHCID 6453107—
SolventDimethylformamideHCID 6228—
SolventTetrahydrofuranHCID 8028—
SolventTriethylamineHCID 8471—
Productcarbobenzoxy-beta-alanyl-L-proline t-butyl esterHCID 54135485—

Reaction Steps

4.46 g. of carbobenzoxy-β-alanine is dissolved in 20 ml. of tetrahydrofuran and the resulting solution cooled to -10° C. With constant stirring of the solution, 2.4 ml. of N-methylmorpholine followed by 2.6 ml. of isobutylchloroformate are added and the resulting reaction mixture is stirred thereafter for approximately 5 minutes at -10° C. 4.16 g. of L-proline t-butyl ester hydrochloride in 20 ml. of dimethylformamide and 2.8 ml. of triethylamine is added to the reaction mixture which is thereafter stirred overnight, while slowly warming to room temperature. The solvent of the reaction mixture is evaporated in vacuo at 30°-35°. The residue is dissolved in 800 ml. of ethyl acetate which is washed with (2×150 ml.) a 10% citric acid solution, with (1×150 ml.) water, with (2×150 ml.) saturated solution of sodium bicarbonate and then with (2×100 ml.) water. The organic layer is dried with anhydrous magnesium sulfate and the solvent evaporated to yield carbobenzoxy-β-alanyl-L-proline t-butyl ester.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04221706
Source datasetuspto-grants-1980_09
ORD IDord-c7cd6af73aca49feafad7a587907044d
Source noteuspto-grants-1980_09