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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1613547Generated: October 26, 2026

1-(2-Tert-butyl-5-methylphenyloxy)-2-butanol → 1-(2-Tert-butyl-5-methylcyclohexyloxy)-2-butanol

https://huagongshe.com/reaction/1613547

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1-(2-Tert-butyl-5-methylphenyloxy)-2-butanolHCID 19774056—
Reactant1-(2-tert-Butylphenoxy)butan-2-olHCID 19774062—
CatalystPalladiumHCID 23938—
Product1-(2-Tert-butyl-5-methylcyclohexyloxy)-2-butanolHCID 1977406163%

Reaction Steps

The synthesis was carried out in the same manner as described in Example 3b, except that 50 g (0.21 mol) of 1-(2-tert-butyl-5-methylphenyloxy)-2-butanol were used instead of 50 g (0.23 mol) of 1-(2-tert-butylphenyloxy)-2-butanol and the amount of the same palladium catalyst was increased to 2.5 g to effect the reaction for 4 hours, to obtain 32 g of 1-(2-tert-butyl-5-methylcyclohexyloxy)-2-butanol (bp. 139° to 140° C./3.5 mm Hg) in a 63% yield.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05194423
Source datasetuspto-grants-1993_03
ORD IDord-7abe08cd101b4a948dbe3654e8927ef9
Source noteuspto-grants-1993_03