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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 248382Generated: October 30, 2026

Sodium borohydride → HCID 86746832, compound

https://huagongshe.com/reaction/248382

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium borohydrideHCID 4311764—
ReactantHCID 19759475HCID 19759475—
Solvent1,2-DichloroethaneHCID 11—
ProductHCID 86746832HCID 86746832142.8%

Reaction Steps

To a solution of 1-(4-ethoxycarbonylphenyl)-4-formylpyrrole-2-carbonitrile (2.0 g) in 1,2-dichloroethane (10 ml) was added sodium borohydride (296 mg) in one portion under nitrogen at ambient temperature. The mixture was stirred for one hour at the same temperature and then quenched with aqueous saturated ammonium chloride solution at 5° C. The organic layer was washed with water and brine, dried, and concentrated in vacuo. The residue was purified by silica gel column chromatography eluted by a mixture of ethyl acetate and n-hexane (2:1) to give 4-ethoxycarbonylphenyl)-4-hydroxymethylpyrrole-2-carbonitrile (1.3 g) as a white solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05210092
Source datasetuspto-grants-1993_05
ORD IDord-56430e99099d45e2a590c5bec9173100
Source noteuspto-grants-1993_05