HuagongsheHuagongshe Chemistry Print Report · For research reference only
Methyl Salicylate → Methyl 2-(1-methoxycarbonylpentoxy)benzoate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Methyl Salicylate | HCID 4133 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | Hexanoic acid, 2-bromo-, methyl ester | HCID 95578 | — |
| Solvent | Acetonitrile | HCID 6342 | — |
| Product | Methyl 2-(1-methoxycarbonylpentoxy)benzoate | HCID 10446375 | — |
Reaction Steps
15.2 g of methyl salicylate and 18.0 g of potassium carbonate were introduced into 125 ml of acetonitrile in a 250 ml flask under an argon atmosphere and, at room temperature, 20.9 g of methyl 2-bromohexanoate were added. The colourless suspension was heated under reflux with stirring for 16 hours, and the progress of the reaction was checked by thin-layer chromatography. After cooling to room temperature, the suspension was filtered and the residue was washed with acetone. Concentration of the filtrate in vacuo resulted in 27.8 g (99% of theory) of methyl 2-(1-methoxycarbonylpentoxy)benzoate as yellow oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06984741B2 |
| Source dataset | uspto-grants-2006_01 |
| ORD ID | ord-414dc2d4881d4e1091e5276df4aa6c33 |
| Source note | uspto-grants-2006_01 |