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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 544594Generated: October 26, 2026

4-tert-Butylphenol → 4-(4-Tert-butylphenoxy)butyl acetate

https://huagongshe.com/reaction/544594

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-tert-ButylphenolHCID 7393—
Reactant1-Butanol, 4-chloro-, 1-acetateHCID 23399—
ReactantSodium hydrideHCID 24758—
ReactantPhenolateHCID 119047—
SolventDimethylformamideHCID 6228—
Product4-(4-Tert-butylphenoxy)butyl acetateHCID 13313736—

Reaction Steps

To a stirred slurry of 1.6 g sodium hydride (as 50% dispersion in oil) in 50 ml dry dimethyl formamide was added, dropwise, a solution of 5.0 g p-tert-butylphenol (33.3 mmoles) in 50 ml dry dimethyl formamide and the solution stirred under nitrogen until the phenoxide had totally formed. To the phenoxide was added a solution of 5.0 g 4-chlorobutyl acetate (33.3 mmoles) in 50 ml dry dimethyl formamide and the solution was stirred for fourteen hours. The reaction mixture was partitioned between water/toluene. The organic layer was removed, washed with water, then 1 N sodium bicarbonate. The organic layer was removed, dried and evaporated to an orange oil, 5.6 g. The oil was chromatographed on 500 g, 90 to 200 mesh silica gel (CH2Cl2 eluent) yielding pure 4-(p-tert-butylphenoxy)-butyl acetate.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04451474
Source datasetuspto-grants-1984_05
ORD IDord-68859b502a7640898737464c79dba6be
Source noteuspto-grants-1984_05