Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Cyclohexyl formate | HCID 20358 | — |
| Reactant | HCID 178506046 | HCID 178506046 | — |
| Solvent | Water | HCID 962 | — |
| Product | Cyclohexanol | HCID 7966 | — |
| Product | Cyclohexyl formate | HCID 20358 | — |
Reaction Steps
Using a procedure analogous to that employed in Example 1, 1.28 g of cyclohexyl formate, 2.70 g of water, and 0.5 g of sulfonated polytetrafluoroethylene were heated at 110° C. over a period of 2 h. Following homogenization of the liquid phase there were obtained, in addition to unconverted cyclohexyl formate, 75.8 mol % of cyclohexanol. The only by-product formed was cyclohexene in a concentration of 0.9 mol %.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05475158 |
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| Source dataset | uspto-grants-1995_12 |
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| ORD ID | ord-14ee170facd645a5b923ffeae4bf936e |
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| Source note | uspto-grants-1995_12 |
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