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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1757685Generated: October 26, 2026

1,2-Butanediol → 2-tert-Butylcyclohexyloxybutanol

https://huagongshe.com/reaction/1757685

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1,2-ButanediolHCID 11429—
Reactant2-tert-ButylcyclohexanoneHCID 102681—
Reactant6-t-Butyl-2-ethyl-1,4-dioxaspiro[4.5]decaneHCID 15789586—
CatalystPalladiumHCID 23938—
CatalystRutheniumHCID 23950—
Product2-tert-ButylcyclohexyloxybutanolHCID 16442289%

Reaction Steps

A 500 ml capacity autoclave was charged with 150 g (0.68 mol) of 6-t-butyl-2-ethyl-1,4-dioxaspiro[4.5]decane which has been prepared from 2-t-butylcyclohexanone and 1,2-butanediol, 1.47 g of a catalyst of 5% palladium supported on active carbon and 0.03 g of a catalyst of 5% ruthenium supported on active carbon. The reaction was carried out under ahydrogen pressure of 70 kg/cm2 and at a temperature of 190° C. for 10 hours until completion of the absorption of hydrogen. In this way, 134.7 g of 1-(2-t-butylcyclohexyloxy)-2-butanol was obtained (yield=89%; cis:trans=66:34).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05446208
Source datasetuspto-grants-1995_08
ORD IDord-c878a16902cb46fdaf879a35f20da910
Source noteuspto-grants-1995_08