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 | — |
Reaction Steps
LiBH4 (5.00 g, 0.23 mmol) was added to a solution of 3-bromo-2-methoxy-benzoic acid methyl ester (10.50 g, 42.80 mmol) in Et2O at 0° C. The reaction mixture was stirred for 5 minutes, MeOH (8.70 mL, 0.22 mmol) was added in a dropwise fashion. The reaction mixture was then stirred for 30 minutes, and was quenched into 1N NaOH. The resulting solution was extracted with Et2O (3×200 mL) and the combined organic phases were washed with brine (1×150 mL), dried over MgSO4 and concentrated to afford the title compound. Spectroscopic data: 1H NMR (300 MHz, CDCl3.) δ 1.68 (t, J=5.86 Hz, 1H), 3.90 (s, 3H), 4.61 (d, J=5.86 Hz, 2H), 6.89 (d, J=8.50 Hz, 1H), 7.25-7.30 (m, J=2.00 Hz, 1H), 7.57 (d, J=2.05 Hz, 1H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08557853B2 |
| Source dataset | uspto-grants-2013_10 |
| ORD ID | ord-bf8ed33c063f48eb988d306d85c06d7e |
| Source note | uspto-grants-2013_10 |