HuagongsheHuagongshe Chemistry Print Report · For research reference only
Benzyl Bromide → Benzyl 3-hydroxytetradecanoate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Benzyl Bromide | HCID 7498 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | (+-)-3-Hydroxytetradecanoic acid | HCID 16064 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | Benzyl 3-hydroxytetradecanoate | HCID 10520747 | — |
Reaction Steps
To a solution of 5.00 g of 3-hydroxymyristic acid in 50 ml of DMF were added at room temperature 2.85 ml of triethylamine and 2.43 ml of benzyl bromide. The reaction mixture was stirred at room temperature overnight. The solvent was removed in vacuo, ethyl acetate and water were added to the residue, and the organic layer was separated, washed twice with water and dried over anhydrous sodium sulfate. After the solvent was removed in vacuo, the crude product was purified by a silica gel column chromatography to afford 3.69 g of benzyl 3-hydroxymyristate (Intermediate 2).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06252041B1 |
| Source dataset | uspto-grants-2001_06 |
| ORD ID | ord-a793d3b1b3ef4d3e974374fe0446f434 |
| Source note | uspto-grants-2001_06 |