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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2260035Generated: November 1, 2026

Cyclohexyl formate → Cyclohexanol

https://huagongshe.com/reaction/2260035

Reaction equation

Participants

RoleNameHCIDCharge
ReactantCyclohexyl formateHCID 20358—
ReactantHCID 178506046HCID 178506046—
SolventWaterHCID 962—
ProductCyclohexanolHCID 7966—
ProductCyclohexyl formateHCID 20358—

Reaction Conditions

Temperature110 °C

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05475158
Source datasetuspto-grants-1995_12
ORD IDord-14ee170facd645a5b923ffeae4bf936e
Source noteuspto-grants-1995_12