Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Water | HCID 962 | — |
| Reactant | Pyridine | HCID 1049 | — |
| Reactant | Cyclohexanol | HCID 7966 | — |
| Reactant | 1-Chloroethyl chloroformate | HCID 521305 | — |
| Solvent | Chloroform | HCID 6212 | — |
| Product | 1-Chloroethyl Cyclohexyl Carbonate | HCID 11229529 | — |
Reaction Steps
Cyclohexanol (4.58 g) was dissolved in chloroform (75 ml), pyridine (3.63 g) was added, and the mixture was cooled to −78° C. 1-Chloroethyl chlorocarbonate (5.0 ml) was added. The reaction mixture was gradually returned to room temperature and stirred for one day. Water was added to the reaction mixture to separate the organic layer. The organic layer was washed successively with water and brine, dried over sodium sulfate, and concentrated under reduced pressure to give the title compound (8.85 g).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07285572B2 |
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| Source dataset | uspto-grants-2007_10 |
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| ORD ID | ord-ca4db84a1ad24c15b5e311f9fec6e374 |
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| Source note | uspto-grants-2007_10 |
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