HuagongsheHuagongshe Chemistry Print Report · For research reference only
Toluene → 4-(Benzyloxy)phenyl 4-(decyloxy)benzoate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Toluene | HCID 1140 | — |
| Reactant | Dichloromethane | HCID 6344 | — |
| Reactant | Monobenzone | HCID 7638 | — |
| Reactant | 4-Decyloxybenzoyl chloride | HCID 11779353 | — |
| Solvent | Diethyl Ether | HCID 3283 | — |
| Solvent | Triethylamine | HCID 8471 | — |
| Product | 4-(Benzyloxy)phenyl 4-(decyloxy)benzoate | HCID 19913443 | 95.3% |
Reaction Steps
4-Benzyloxyphenol (20.0 g. 100 mmol) was dissolved in 200 mL dry ether and 10 mL triethylamine. 4-Decyloxybenzoyl chloride (30.0 g, 100 mmol) was added dropwise with stirring at room temperature under nitrogen. After 1 day of stirring at room temperature under nitrogen atmosphere, 200 mL toluene and 200 mL methylene chloride were added to the reaction mixture. The reaction mixture was then filtered and the filtrate washed twice with 0.5N HCl, once with water, and dried over anhydrous magnesium sulfate, filtered, and concentrated under reduced pressure. The crude product was recrystallized from toluene-ethanol to provide 43.9 g (95% yield) 4-benzyloxyphenyl 4-decyloxybenzoate.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05082587 |
| Source dataset | uspto-grants-1992_01 |
| ORD ID | ord-914f96f867904f4f853a847747301ff4 |
| Source note | uspto-grants-1992_01 |