HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 894519Generated: October 30, 2026
Thionyl Chloride → HCID 19995701, compound
https://huagongshe.com/reaction/894519
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Thionyl Chloride | HCID 24386 | — |
| Reactant | Phosphorus oxychloride | HCID 24813 | — |
| Reactant | HCID 23422127 | HCID 23422127 | — |
| Reactant | HCID 54038390 | HCID 54038390 | — |
| Reactant | HCID 178524845 | HCID 178524845 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | HCID 19995701 | HCID 19995701 | — |
Reaction Steps
o-Halogeno-(hetero-)aryl-carboxylic acid halides which can be employed in the process according to the invention, and processes for their preparation, are known. Thus, for example, J. Am. Chem. Soc. 40,233 (1908) describes the preparation of 2-ethylmercapto-6-chloropyrimidine-5-carboxylic acid chloride by reacting 2-ethylmercapto-4-oxo-3,4-dihydropyrimidine-5-carboxylic acid with phosphorus oxychloride. The reaction of 2-hydroxy-quinoxaline-3-carboxylic acid with thionyl chloride in the presence of a catalytic amount of dimethylformamide to give 2-chloroquinoxaline-3-carboxylic acid chloride is described in Arch. Pharm. 306, 401 (1973). The reaction of 4-chloronicotinic acid with thionyl chloride under reflux to give 4-chloronicotinic acid chloride is described in J. Chem. Soc. (C), 1966, 1816.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04284629 |
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| Source dataset | uspto-grants-1981_08 |
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| ORD ID | ord-20f978b35d86413390c9f5150ecd54fd |
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| Source note | uspto-grants-1981_08 |
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