Participants
| Role | Name | HCID | Charge |
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| Reactant | Phosgene | HCID 6371 | — |
| Reactant | Cyclohexane, (ethenyloxy)- | HCID 75129 | — |
| Product | 3-Cyclohexyloxyacryloyl chloride | HCID 53968361 | 88% |
Reaction Steps
50 g (0.5 mol) of phosgene were condensed into a stirred apparatus fitted with a -78° C. dry-ice condenser. 50.5 g (0.4 mol) of cyclohexyl vinyl ether were subsequently added dropwise at 20° C. over the course of 3 hours. The mixture was subsequently stirred at 50° C. for a further 5 hours. The excess phosgene was expelled by means of nitrogen, and the crude product was worked up by distillation at 110° C./2.5 mbar, giving 66.4 g (88%) of valuable product.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05543568 |
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| Source dataset | uspto-grants-1996_08 |
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| ORD ID | ord-ecf4353b466d4d758c7ac9da0a4501a6 |
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| Source note | uspto-grants-1996_08 |
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