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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1499921Generated: November 2, 2026

Sodium borohydride → 6-Chloro-3-ethoxy-4-(1-hydroxyethyl)-2-pyrrolidin-1-ylbenzonitrile

https://huagongshe.com/reaction/1499921

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium borohydrideHCID 4311764—
Reactant4-Acetyl-6-chloro-3-ethoxy-2-pyrrolidin-1-ylbenzonitrileHCID 86677838—
SolventMethanolHCID 887—
SolventEthyl AcetateHCID 8857—
Product6-Chloro-3-ethoxy-4-(1-hydroxyethyl)-2-pyrrolidin-1-ylbenzonitrileHCID 86677839101.8%

Reaction Steps

The 4-acetyl-6-chloro-3-ethoxy-2-pyrrolidin-1-ylbenzonitrile (0.045 g, 0.15 mmol) was dissolved in methanol (3 mL) and cooled in an ice bath. The sodium tetrahydroborate (0.0058 g, 0.15 mmol) was added and the reaction was monitored by LC/MS. After stirring for 1 h, the reaction was taken up in ethyl acetate and washed with water, sodium bicarbonate, brine and dried over magnesium sulfate to give crude 6-chloro-3-ethoxy-4-(1-hydroxyethyl)-2-pyrrolidin-1-ylbenzonitrile as a clear oil (0.045 g, 100%). LCMS calculated for C15H20ClN2O2(M+H)+: m/z=295.1; found 295.1.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09199982B2
Source datasetuspto-grants-2015_12
ORD IDord-5ef09705cc1f48f59ba7db685d706ba6
Source noteuspto-grants-2015_12