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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 323170Generated: October 29, 2026

Hydrochloric Acid → HCID 22011008, compound

https://huagongshe.com/reaction/323170

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantSodium borohydrideHCID 4311764—
ReactantHCID 22010672HCID 22010672—
SolventEthanolHCID 702—
SolventEthyl AcetateHCID 8857—
ProductHCID 22011008HCID 2201100876.3%

Reaction Steps

To a solution of 4-(4′-methylbiphenyl-2-carboxamido)-N-ethoxycarbonylmethyl-N-(2-methylphenyl)benzamide (100 mg) in ethanol (5 ml) was added sodium borohydride (37 mg) at 0° C. and the mixture was stirred for 2 hours at ambient temperature. Since the reaction was not completed and it was so slow, sodium borohydride (220 mg) was added to the mixture at 0° C. and stirred overnight. The reaction mixture was neutralized with 1N hydrochloric acid and diluted with ethyl acetate. The organic layer was washed with brine and dried over magnesium sulfate. Filtering and the removal of solvents afforded 4-(4′-methylbiphenyl-2-carboxamido)-N-(2-hydroxyethyl)-N-(2-methylphenyl)benzamide (70 mg) as a colorless prisms.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06211242B1
Source datasetuspto-grants-2001_04
ORD IDord-3b67006252cb49ef84005d989d1e1616
Source noteuspto-grants-2001_04