HuagongsheHuagongshe Chemistry Print Report · For research reference only
Benzoyl chloride → 4-Benzyloxy-3-chloro-5-methyl-1-benzoyloxybenzene
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Benzoyl chloride | HCID 7412 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | 4-Benzyloxy-3-chloro-5-methylphenol | HCID 18504631 | — |
| Solvent | Chloroform | HCID 6212 | — |
| Product | 4-Benzyloxy-3-chloro-5-methyl-1-benzoyloxybenzene | HCID 18504554 | 90.6% |
Reaction Conditions
| Temperature | 0 °C |
|---|
Reaction Steps
To a solution of 27.3 g of 4-benzyloxy-3-chloro-5-methylphenol dissolved in 250 ml of chloroform and being stirred at 0° C. were added 15.4 g of benzoyl chloride and then 13.3 g of triethylamine. After stirring at room temperature for 2 hours, the chloroform layer was washed with water, dried with anhydrous magnesium sulfate, and concentrated. The residue was subjected to silica gel chromatography, which afforded 35 g of 4-benzyloxy-3-chloro-5-methyl-1-benzoyloxybenzene (90% yield).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06376428B1 |
| Source dataset | uspto-grants-2002_04 |
| ORD ID | ord-1009c6bf688041aca4124d407d3ebeff |
| Source note | uspto-grants-2002_04 |