Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Sulfur Dioxide | HCID 1119 | — |
| Reactant | Thionyl Chloride | HCID 24386 | — |
| Reactant | HCID 53861785 | HCID 53861785 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | Thionyl Chloride | HCID 24386 | — |
| Product | HCID 53664299 | HCID 53664299 | — |
Reaction Steps
An agitated flask is charged with 800 g (6.72 mole) of thionyl chloride together with 2 ml of dimethylformamide as accelerator; the mixture is heated under agitation to 50° C. and, within 2 hours, 350 g (1.56 mol) of crystalline 2,3,4,4-tetrachloro-2-butenoic acid is added in incremental portions. During this step a strong evolution of gas occurs. After the addition has been completed, the mixture is heated for 1-2 hours to boiling (79° C.) until the evolution of sulfur dioxide and hydrogen chloride has ceased (bubble counter at the cooler outlet). Thereafter the reaction mixture is distilled over a 10 cm column, thus obtaining 604 g (5.07 mol) of unreacted thionyl chloride and 359 g (1.48 mol) of 2,3,4,4-tetrachloro-2-butenoic acid chloride; b.p. 102° C./26 mbar; nD20 =1.5478. Yield: 95% of theory.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04361686 |
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| Source dataset | uspto-grants-1982_11 |
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| ORD ID | ord-05f166227bb244a08fb725b0b2fbf0b6 |
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| Source note | uspto-grants-1982_11 |
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