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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1586804Generated: November 1, 2026

Sodium borohydride → HCID 19759235, compound

https://huagongshe.com/reaction/1586804

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium borohydrideHCID 4311764—
ReactantHCID 19759475HCID 19759475—
Solvent1,2-DichloroethaneHCID 11—
ProductHCID 19759235HCID 1975923564.5%

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 1-(4-ethoxycarbonylphenyl)-4-hydroxymethylpyrrole-2-carbonitrile (1.3 g) as a white solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05215994
Source datasetuspto-grants-1993_06
ORD IDord-d9da9fe9f1e4454caac7c319d1098224
Source noteuspto-grants-1993_06