HuagongsheHuagongshe Chemistry Print Report · For research reference only
Methanol → Methyl 4-bromo-2-methylbenzoate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Methanol | HCID 887 | — |
| Reactant | 4-Bromo-2-methylbenzoic acid | HCID 99570 | — |
| Product | Methyl 4-bromo-2-methylbenzoate | HCID 22031226 | 89% |
Reaction Steps
To a round bottomed flask was added MeOH (25 mL) and commercially available 4-bromo-2-methyl benzoic acid (7.0 g, 32.8 mmol). Then 4N HCL/dioxanes (25 mL) was added to the insoluble mixture and stirred under reflux for 3 h. The reaction was concentrated. EtOAc and H2O were added to the slurry and partitioned. The EtOAc layer was washed with NaHCO3 (sat.) 3×, washed with brine and dried with Na2SO4 and concentrated to give methyl 4-bromo-2-methylbenzoate as a light brown oil (6.7 g, 89% yield).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08242129B2 |
| Source dataset | uspto-grants-2012_08 |
| ORD ID | ord-2819b18bfab447fda7133affecf7ee68 |
| Source note | uspto-grants-2012_08 |