Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Thionyl Chloride | HCID 24386 | — |
| Reactant | Chlorosuccinimide | HCID 31398 | — |
| Reactant | HCID 13100663 | HCID 13100663 | — |
| Product | HCID 12659717 | HCID 12659717 | 82% |
Reaction Steps
To a solution of 343.2 g (1 mole) of 4,4,4-tribromobutyric acid chloride in 600 g of thionylchloride 266.0 g (2 mole) of N-chlorosuccinimide is added portion wise at 60° C. while the reaction mixture is irradiated with a mercury high-pressure lamp. After addition of the N-chlorosuccinimide the reaction mixture is stirred for 5 hours at 60° C. while irradiation is continued. Then the thionyl chloride is evaporated and the residue is distilled in vacuo. 309.7 (82% of theory) of 2-chloro-4,4,4-tribromobutyric acid chloride, b.p. 59°-63° C./0.05 torr is obtained.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04322374 |
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| Source dataset | uspto-grants-1982_03 |
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| ORD ID | ord-bd702034666d4231a7aec2d3d3bbbf54 |
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| Source note | uspto-grants-1982_03 |
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