HuagongsheHuagongshe Chemistry Print Report · For research reference only
Methanol → 3-Bromo-2-methoxybenzenemethanol
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Methanol | HCID 887 | — |
| Reactant | Lithium borohydride | HCID 4148881 | — |
| Reactant | Methyl 3-bromo-2-methoxybenzoate | HCID 46311082 | — |
| Solvent | Diethyl Ether | HCID 3283 | — |
| Product | 3-Bromo-2-methoxybenzenemethanol | HCID 17750316 | 85.2% |
Reaction Steps
2.4 g of lithium borohydride (LiBH4) was added to a solution of 5.3 g of 3-bromo-2-methoxy-benzoic acid methyl ester 5 in 200 mL of ether (Et2O) at 0° C. After stirring for 5 minutes, 5 mL of methanol was added. The reaction mixture was warmed to room temperature and kept there for 2.5 hours. Thereafter, 2.4 g more of lithium borohydride was added. The reaction mixture was quenched with aluminum chloride. After standard aqueous work up, and silica gel column purification (hexane/ethyl acetate 2:1), 4.0 g of 3-bromo-2-methoxy-phenyl-methanol 6 was obtained.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08071636B2 |
| Source dataset | uspto-grants-2011_12 |
| ORD ID | ord-a931a1fc30d84835809a4d2f1b5fc70f |
| Source note | uspto-grants-2011_12 |