HuagongsheHuagongshe Chemistry Print Report · For research reference only
Water → 4-(Benzyloxy)-2-tert-butylphenol
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Water | HCID 962 | — |
| Reactant | Benzyl Chloride | HCID 7503 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | Tert-Butylhydroquinone | HCID 16043 | — |
| Solvent | 2-Methoxyethanol | HCID 8019 | — |
| Product | 4-(Benzyloxy)-2-tert-butylphenol | HCID 12423646 | — |
Reaction Steps
To a stirred solution of t-butyl hydroquinone (1.0 Kg) in 2-methoxy ethanol (2.0 L), was charged K2CO3 (2.0 Kg) portionwise under nitrogen atmosphere and the mixture refluxed. Benzyl chloride (0.762 L) was added dropwise at reflux temperature and heated further for 1.5 hr. The progress of the reaction was monitored on TLC. The reaction mixture was cooled and added DM Water (6.0 L). The uppermost oily layer was separated, dissolved in ethyl acetate (3.4 L), and washed with DM water (3.4 L×3). The uppermost oily layer was separated, dried over sodium sulfate and evaporated to dryness to give the crude title compound (1.5 Kg). The crude product was employed in the next step without further purification,
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07825257B1 |
| Source dataset | uspto-grants-2010_11 |
| ORD ID | ord-af631e3ece794fdd851f76755404db6f |
| Source note | uspto-grants-2010_11 |