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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2372638Generated: October 31, 2026

Hydrochloric Acid → HCID 67896332, compound

https://huagongshe.com/reaction/2372638

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantMethanolHCID 887—
ReactantSodium HydroxideHCID 14798—
ReactantHCID 53936874HCID 53936874—
ReactantHCID 131717209HCID 131717209—
SolventWaterHCID 962—
ProductHCID 67896332HCID 67896332—

Reaction Steps

A mixture of N-(1-oxo-3-phenylpropyl)-3-[(phenylmethoxy)methyl]-L-histidine, methyl ester (17.2 g., 40.8 mmole) and aqueous sodium hydroxide solution (52 ml. of 1.0N solution, 52 mmole) in methanol (42 ml.) was stirred at 25° for 6 hours, after which it was diluted with water (500 ml.) and washed with ethyl acetate. The aqueous phase was neutralized by the addition of 1.0N hydrochloric acid (52 ml., 52 mmole, resulting pH of 5) and the mixture was extracted with ethyl acetate (5 times). Both the extracts and the aqueous wash were concentrated in vacuo. Each of the concentrates was stirred with hot isopropanol (500 ml. each) and filtered while hot. The filtrates were combined and partially concentrated until crystals formed. The crystals were collected and dried to give 6.5 g. of N-(1-oxo-3-phenylpropyl)-3-[(phenylmethoxy)-methyl]-L-histidine as a white powder; m.p. 163°-165°.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05098924
Source datasetuspto-grants-1992_03
ORD IDord-b2fcb25d68bc4be4b7db65bdd90d5be0
Source noteuspto-grants-1992_03