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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1194833Generated: October 26, 2026

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

https://huagongshe.com/reaction/1194833

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 1N 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 numberUS04816491
Source datasetuspto-grants-1989_03
ORD IDord-2f9e50a2b82f45cb8758d3fe71ba23f7
Source noteuspto-grants-1989_03