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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 47047Generated: October 25, 2026

Sodium Hydroxide → HCID 54110235, compound

https://huagongshe.com/reaction/47047

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium HydroxideHCID 14798—
ReactantCyclohexanecarbonyl chlorideHCID 75938—
ReactantL-alanyl-L-proline ethylamide hydrobromideHCID 70602162—
SolventDichloromethaneHCID 6344—
ProductHCID 54110235HCID 5411023560%

Reaction Steps

1.25 g (0.00425 mol) of L-alanyl-L-proline ethylamide hydrobromide were suspended in 20 ml of dichloromethane and to the suspension were added 17.84 ml (0.00892 mol) of 0.5-N sodium hydroxide solution followed by 0.62 ml (1.1 equivalents) of cyclohexane carboxylic acid chloride. The mixture was stirred vigorously for 1 hour. The solution was diluted with 80 ml of dichloromethane, the organic layer was separated, washed with 60 ml of brine, dried over magnesium sulphate and evaporated to give a solid. Recrystallisation from ethyl acetate yielded 0.83 g (60%) of N-cyclohexylcarbonyl-L-alanyl-L-proline ethylamide of melting point 190.5°-191.5° C.; [α]D20 =-116.0° (c=1.055% in methanol).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04176116
Source datasetuspto-grants-1979_11
ORD IDord-ee71e4b6f4b54c56a0a6aad5f6d89a52
Source noteuspto-grants-1979_11