Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Thionyl Chloride | HCID 24386 | — |
| Reactant | Paraldehyde | HCID 31264 | — |
| Reactant | HCID 178511260 | HCID 178511260 | — |
| Catalyst | Zincchloride | HCID 3007855 | — |
| Product | HCID 178456134 | HCID 178456134 | — |
Reaction Steps
trans-4-cyanocyclohexanecarboxylic acid (7.7 g; 0.05 mol) and thionyl chloride (8.0 g; 0.066 mol) was mixed and refluxed for 30 min. Excess thionyl chloride was evaporated in vacuum. Paraldehyde (2.5 g; 0.062 mol) and a catalytic amount of zinc chloride were added and the mixture was heated at 90° C. for 11/2 h with stirring. The cooled mixture was extracted with ether, washed with sodium bicarbonate solution, dried and evaporated, the product was distilled at 112° C./1 Pa. Yield 6.5 g of an oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04483867 |
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| Source dataset | uspto-grants-1984_11 |
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| ORD ID | ord-a1a67fbbe0ec4259a7575c8a2ea8e56f |
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| Source note | uspto-grants-1984_11 |
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