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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2260036Generated: October 30, 2026

Cyclohexyl formate → Cyclohexanol

https://huagongshe.com/reaction/2260036

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, 1.8 g of water, and 0.5 g of a sulfonated polytetrafluoroethylene were heated at 110° C. over a period of 2 h. Following separation of the catalyst and homogenization with acetone there were obtained, in addition to unconverted cyclohexyl formate, 70.2 mol % of cyclohexanol, and the only by-product was 1.8 mol % of cyclohexene.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05475158
Source datasetuspto-grants-1995_12
ORD IDord-31231c9307f342118c2a247229c11b9e
Source noteuspto-grants-1995_12