Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Sodium Iodide | HCID 5238 | — |
| Reactant | Cyclohexanecarbonyl chloride | HCID 75938 | — |
| Solvent | Acetonitrile | HCID 6342 | — |
| Product | HCID 12715979 | HCID 12715979 | 61.6% |
Reaction Steps
In 80 ml of acetonitrile is dissolved 6 g of sodium iodide and, then, 5 g of cyclohexanecarbonyl chloride is added dropwise to the solution under ice-cooling. This mixture is stirred at 0° C. for 30 minutes. Then, insoluble matters are removed by filtration and the filtrate is concentrated under reduced pressure. To the residue is added 20 ml of petroleum ether and insoluble matters are removed by filtration and the filtrate is subjected to distillation under reduced pressure to obtain 5.0 g of cyclohexanecarbonyl iodide. Yield: 61%. B.p. 75°-80° C./5 mmHg [b.p. 103°-105° C./11 mmHg according to "Bull. Chem. Soc. Japan" 34, 480 (1961)].
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04593115 |
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| Source dataset | uspto-grants-1986_06 |
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| ORD ID | ord-c096086307c64966857f53bf05c3712b |
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| Source note | uspto-grants-1986_06 |
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