Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 47045Generated: October 25, 2026

Benzoyl chloride → N-benzoyl-L-alanyl-L-proline ethylamide

https://huagongshe.com/reaction/47045

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzoyl chlorideHCID 7412—
ReactantSodium HydroxideHCID 14798—
ReactantL-alanyl-L-proline ethylamide hydrobromideHCID 70602162—
SolventDichloromethaneHCID 6344—
ProductN-benzoyl-L-alanyl-L-proline ethylamideHCID 5430997968.9%

Reaction Steps

1.42 g (0.0048 mol) of L-alanyl-L-proline ethylamide hydrobromide were dissolved in 20 ml of methylene chloride, 21.8 ml (0.01 mol) of 0.5-N sodium hydroxide solution were added followed by 0.54 ml (0.0053 mol) of benzoyl chloride. The mixture was stirred vigorously at room temperature for 1 hour with care being taken that the solution remained basic, this being achieved by the addition of a few drops of 0.5-N sodium hydroxide solution. The layers were then allowed to separate and the methylene chloride layer was separated, dried over magnesium sulphate and evaporated to an oil which crystallised on treatment with ethyl acetate. The crystals were filtered off, washed and dried to yield 1.05 g of N-benzoyl-L-alanyl-L-proline ethylamide of melting point 200°-202° C.; [α]D20 =-82.7° (c=0.99 in methanol).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04176116
Source datasetuspto-grants-1979_11
ORD IDord-00cb2a1f19a44f2d8f439eb07dc5a70f
Source noteuspto-grants-1979_11