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 3-hydroxymyristic acid (5.00 g) and triethylamine (2.85 g) in DMF (50 ml) was added benzyl bromide (2.43 ml) and the mixture was stirred at room temperature overnight. After the solvent was removed in vacuo, to the residue were added ethyl acetate and water. The separated ethyl acetate layer was washed twice with water and then dried over anhydrous sodium sulfate. After the ethyl acetate was removed in vacuo, purification was carried out by a silica gel column chromatography (silica gel 30 g, chloroform:methanol=100:0-10) to afford 3.69 g of benzyl 3-hydroxymyristate.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06858585B1 |
| Source dataset | uspto-grants-2005_02 |
| ORD ID | ord-e8fb2a66ea7c487f8f69063cb844a64a |
| Source note | uspto-grants-2005_02 |