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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1731780Generated: October 25, 2026

Thionyl Chloride → 3,4,5-Trihydroxybenzonitrile

https://huagongshe.com/reaction/1731780

Reaction equation

Participants

RoleNameHCIDCharge
ReactantThionyl ChlorideHCID 24386—
Reactant3,4,5-TrihydroxybenzamideHCID 69256—
SolventEthyl AcetateHCID 8857—
Product3,4,5-TrihydroxybenzonitrileHCID 1374683586%

Reaction Conditions

Temperature90 °C

Reaction Steps

A reaction mixture containing 23.5 g. of gallamide, 180 ml. of ethyl acetate and 35 ml. of thionylchloride was refluxed for about 18 hours. The volatile contents were removed by evaporation in vacuo and the resulting residue dissolved in 215 ml. of water. This aqueous solution was heated to about 90° C. until the evolution of gas had ceased. The aqueous solution was filtered through charcoal and the water removed from the filtrate by evaporation. 18 g. of gallonitrile were obtained melting at about 219° C. with decomposition (86% yield). Other nitriles useful as starting materials can be prepared similarly.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04623659
Source datasetuspto-grants-1986_11
ORD IDord-35d974ef12da44cf8d8830ca5f50aa58
Source noteuspto-grants-1986_11