HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2165969Generated: October 25, 2026
Thionyl Chloride → 3,4,5-Trihydroxybenzonitrile
https://huagongshe.com/reaction/2165969
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Thionyl Chloride | HCID 24386 | — |
| Reactant | 3,4,5-Trihydroxybenzamide | HCID 69256 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | 3,4,5-Trihydroxybenzonitrile | HCID 13746835 | 86% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04942253 |
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| Source dataset | uspto-grants-1990_07 |
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| ORD ID | ord-5b5f25eafe7642dd8bc0aa312c13b930 |
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| Source note | uspto-grants-1990_07 |
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