HuagongsheHuagongshe Chemistry Print Report · For research reference only
Benzyl Chloride → 1-Benzyloxy-2-tert-butyl-4-methyl-benzene
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Benzyl Chloride | HCID 7503 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | 2-tert-Butyl-4-methylphenol | HCID 17004 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | 1-Benzyloxy-2-tert-butyl-4-methyl-benzene | HCID 50886343 | — |
Reaction Steps
8 g of 2-tert-Butyl-4-methyl-phenol (49 mmol) and 16.36 g of potassium carbonate (58 mmol) were stirred in 120 ml DMF until a suspension was formed. 6.74 ml of benzylchloride were then added dropwise and the reaction mixture was stirred for 24 h at RT. After two hours heating at 60° C., the reaction mixture was cooled to RT, filtered off, diluted with ethyl acetate, and washed with water followed by brine. The organic phase was dried over magnesium sulphate, filtered off and concentrated under vacuo. The residue was purified by flash column chromatography (heptane/AcOEt 98/2) to give 8.647 g of a colorless liquid. MS (ISP) 255.3 (M+H)+.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07745477B2 |
| Source dataset | uspto-grants-2010_06 |
| ORD ID | ord-8cdae5bcb04442f4acfe2417bcb9c0c9 |
| Source note | uspto-grants-2010_06 |