Cyclohexyl formate → Cyclohexanol

HRID 2260035Notes

Reaction equation

HRID 2260035 reaction equation
[CH:1]([O:3][CH:4]1[CH2:9][CH2:8][CH2:7][CH2:6][CH2:5]1)=[O:2]>O>[CH:1]([O:3][CH:4]1[CH2:9][CH2:8][CH2:7][CH2:6][CH2:5]1)=[O:2].[CH:4]1([OH:3])[CH2:9][CH2:8][CH2:7][CH2:6][CH2:5]1

Participants

5

Reactant 2

HCID 20358Cyclohexyl formateHCID 178506046HCID 178506046, compound

Product 2

HCID 7966CyclohexanolHCID 20358Cyclohexyl formate

Reagents, catalysts & solvents 1

HCID 962WaterSolvent

Conditions

Temperature
110 °C

Procedure

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 %.

Sources & evidence

ORD record
ord-14ee170facd645a5b923ffeae4bf936e
Source dataset
uspto-grants-1995_12
Patent number
US05475158

Reaction notes

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