HuagongsheHuagongshe Chemistry Print Report · For research reference only
1-Bromooctadecane → 3-Hydroxy-5-(octadecyloxy)benzoic acid phenylmethyl ester
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 1-Bromooctadecane | HCID 8218 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | HCID 11299537 | HCID 11299537 | — |
| Solvent | Acetone | HCID 180 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | 3-Hydroxy-5-(octadecyloxy)benzoic acid phenylmethyl ester | HCID 15233476 | 36% |
Reaction Steps
A mixture of 30 g (0.123 mol) of 3,5-dihydroxybenzoic acid phenylmethyl ester, 40.9 g (0.123 mol) of 1-bromooctadecane, 17 g (0.123 mol) of anhydrous potassium carbonate in 500 ml of acetone and 10 ml of DMF was stirred at reflux for 25 hours. The reaction mixture was filtered and the filtrate was concentrated at reduced pressure to a solid. The residue was treated with water and the product was extracted with methylene chloride. The dried extract was concentrated at reduced pressure to a solid which was purified by HPLC using 1% ethyl acetate-methylene chloride to give 22 g (36% yield, mp 72°-75°) of 3-hydroxy-5-(octadecyloxy)benzoic acid phenylmethyl ester. The structure was confirmed by nmr and mass spectra.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05298652 |
| Source dataset | uspto-grants-1994_03 |
| ORD ID | ord-ab294117e5ce4f7cbb10f82e43eb63d4 |
| Source note | uspto-grants-1994_03 |