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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 717758Generated: October 30, 2026

Sodium borohydride → 2-(4-Fluorophenyl)-3-(5-methyl-2-nitrophenyl)propanenitrile

https://huagongshe.com/reaction/717758

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium borohydrideHCID 4311764—
Reactant(Z)-2-(4-fluorophenyl)-3-(5-methyl-2-nitrophenyl)acrylonitrileHCID 67372031—
SolventMethanolHCID 887—
SolventWaterHCID 962—
SolventTetrahydrofuranHCID 8028—
Product2-(4-Fluorophenyl)-3-(5-methyl-2-nitrophenyl)propanenitrileHCID 6737336499.6%

Reaction Steps

To a cooled solution of (Z)-2-(4-fluorophenyl)-3-(5-methyl-2-nitrophenyl)acrylonitrile (3.0 g, 0.0106 mol) in THF (25 mL) and MeOH (75 mL) was added sodium borohydride (0.808 g, 0.0212 mol) at 0° C. under nitrogen atmosphere. The reaction mixture was stirred for 2 h at RT. After completion of reaction (monitored by TLC), the mixture was diluted with water (100 mL), and extracted with EtOAc (3×150 mL). The organic layer was dried over anhydrous sodium sulfate, and the solvent was removed under reduced pressure to obtain product as a yellow colored solid (3 g, 99% yield).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09193728B2
Source datasetuspto-grants-2015_11
ORD IDord-32405b6382d74a849e2b5ae87da2089c
Source noteuspto-grants-2015_11