HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 5008Generated: October 23, 2026
4-tert-Butylphenol → 4-(4-Tert-butylphenoxy)butyl acetate
https://huagongshe.com/en/reaction/5008
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 4-tert-Butylphenol | HCID 7393 | — |
| Reactant | 1-Butanol, 4-chloro-, 1-acetate | HCID 23399 | — |
| Reactant | Sodium hydride | HCID 24758 | — |
| Reactant | Phenolate | HCID 119047 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | 4-(4-Tert-butylphenoxy)butyl acetate | HCID 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, drop-wise, 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
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US05242936 |
|---|
| Source dataset | uspto-grants-1993_09 |
|---|
| ORD ID | ord-cebef95bc8384043b4a84d71a6aab475 |
|---|
| Source note | uspto-grants-1993_09 |
|---|