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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1632382Generated: November 2, 2026

Hydrochloric Acid → HCID 67915300, compound

https://huagongshe.com/reaction/1632382

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantEthyl alpha-oxobenzenebutanoateHCID 562087—
ReactantSodium cyanoborohydrideHCID 5003444—
ReactantHCID 13132291HCID 13132291—
SolventEthanolHCID 702—
SolventWaterHCID 962—
ProductHCID 67915300HCID 67915300—

Reaction Steps

L-Alanyl-N-(indan-2-yl)-β-alanine (2.0 g) is dissolved in a mixture of 20 ml of water and 100 ml of ethanol, 10 g of ethyl 2-oxo-4-phenylbutyrate is added, and a solution of 0.94 g of sodium cyanoborohydride in 20 ml of ethanol is added dropwise over 2 hours. The mixture is stirred at room temperature for 3 hours and then adjusted to pH 4.0 with 10% hydrochloric acid, and the ethanol is distilled off under reduced pressure. The residue is extracted with 200 ml of ethyl acetate, washed with water and dried, and the ethyl acetate is distilled off under reduced pressure. The residue is dissolved in 2 ml of 20% ethanolic hydrochloric acid, 100 ml of ethyl ether is added, and the mixture is allowed to stand at room temperature. Thus is obtained 1.2 g of N-(1-ethoxycarbonyl-3-phenylpropyl)-L-alanyl-N-(indan-2-yl)-β-alanine hydrochloride as colorless amorphous powder.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04474692
Source datasetuspto-grants-1984_10
ORD IDord-530399c209fd4b37905f2ca6efe77d3a
Source noteuspto-grants-1984_10