Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Chloral | HCID 6407 | — |
| Reactant | Cyclohexene | HCID 8079 | — |
| Reactant | Aluminum(III) Chloride | HCID 6451240 | — |
| Product | HCID 12418397 | HCID 12418397 | 65.4% |
Reaction Steps
Anhydrous aluminum chloride (8.4 g; 0.063 mole) was added portionwise over a period of 2 hours to a stirred mixture of cyclohexene (108 g; 1.32 moles) and chloral (97 g; 0.653 mole), the temperature of which was maintained at 0° C. The reaction was allowed to proceed for a further 1 hour at 0° C. and then poured into a mixture of ice and concentrated hydrochloric acid. The reaction mixture was extracted three times with ether and the combined extracts washed with water (2×200 ml). The dried (MgSO4) extract was evaporated and the residue distilled to give crude product (116 g; 85% purity as judged by G.L.C.), b.p. 90°-94° C./0.1 mm. The crude product was redistilled through a Widmer column to give 1-(2-cyclohexen-1-yl)-2,2,2-trichloroethanol (98 g; 65% yield based on chloral; 93% purity as judged by G.L.C.) b.p. 67°-68° C./0.03 mm. A sample was redistilled for analysis.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04249015 |
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| Source dataset | uspto-grants-1981_02 |
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| ORD ID | ord-810fbbe7af7b46b4b4fbf35f135ef7ad |
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| Source note | uspto-grants-1981_02 |
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