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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 431866Generated: November 1, 2026

Boron Trichloride → Methyl 3-cyano-5-hydroxybenzoate

https://huagongshe.com/reaction/431866

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBoron TrichlorideHCID 25135—
ReactantMethyl 3-(allyloxy)-5-cyanobenzoateHCID 21942395—
CatalystTetrabutylammonium IodideHCID 67553—
SolventDichloromethaneHCID 6344—
ProductMethyl 3-cyano-5-hydroxybenzoateHCID 2194242167%

Reaction Steps

A mixture of methyl 3-allyloxy-5-cyanobenzoate (1.5 g, 6.9 mmol) and tetrabutylammonium iodide (2.8 g, 7.6 mmol) in dichloromethane (38 mL) at −78° C., under argon, was treated with a solution of 1M boron trichloride in dichloromethane (24 mL, 24 mmol). After 5 minutes at −78° C., the reaction mixture was stirred at ambient temperature for 1 hour. The reaction was then quenched with ice water and stirred for an additional 30 minutes. The organic layer was washed with saturated sodium bicarbonate, dried over anhydrous sodium sulfate, filtered and concentrated. Silica gel chromatography using a gradient of 20-30% ethyl acetate/hexanes afforded 811 mg (67%) of methyl 3-cyano-5-hydroxybenzoate as a light yellow solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06660753B2
Source datasetuspto-grants-2003_12
ORD IDord-6ae0c2f14a0741a59f29d02fc98375c3
Source noteuspto-grants-2003_12