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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1421739Generated: October 29, 2026

Lithium borohydride → 2-(2,2,2-Trifluoro-ethoxy)-4-hydroxymethyl-benzonitrile

https://huagongshe.com/reaction/1421739

Reaction equation

Participants

RoleNameHCIDCharge
ReactantLithium borohydrideHCID 4148881—
Reactant4-Cyano-3-(2,2,2-trifluoro-ethoxy)-benzoic acid methyl esterHCID 54349795—
SolventTetrahydrofuranHCID 8028—
Product2-(2,2,2-Trifluoro-ethoxy)-4-hydroxymethyl-benzonitrileHCID 18779688—

Reaction Conditions

Temperature70 °C

Reaction Steps

4-Cyano-3-(2,2,2-trifluoro-ethoxy)-benzoic acid methyl ester from step 1 (1.6 g, 6.2 mmol ) was dissolved in THF (62 ml). LiBH4 in THF (2 M, 6.2 ml, 12.4 mmol) was added. The reaction mixture was heated to 70° C. for 3 hours. The reaction was quenched carefully with 3N HCl and then extracted with EtOAc (3×10 mL). The organic layers were combined, washed with brine, dried (MgSO4) filtered and concentrated to yield the desired product.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06077853
Source datasetuspto-grants-2000_06
ORD IDord-a648bc5b99324135824d815245a532d2
Source noteuspto-grants-2000_06