HuagongsheHuagongshe Chemistry Print Report · For research reference only
2-Bromo-4-chlorobenzoic acid → (2-Bromo-4-chlorophenyl)methanol
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 2-Bromo-4-chlorobenzoic acid | HCID 33126 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | (2-Bromo-4-chlorophenyl)methanol | HCID 54049764 | 85% |
Reaction Steps
Added BH3 (1M in THF, 40 mL) to a solution of 2-bromo-4-chlorobenzoic acid (3.14 g, 13.33 mmol) in THF (3 mL) drop wise at 0° C. The reaction mixture was stirred at room temperature overnight. Extracted with ethyl acetate twice, and washed the organic phase with brine and dried with anhydrous Na2SO4, concentrated to give the title compound (2.5 g, 85%). 1H NMR (300 MHz, CDCl3): δ 4.72 (2H, s), 7.32 (1H, dd, J=1.8 Hz, 8.1 Hz), 7.43 (1H, d, J=8.1 Hz), 7.56 (1H, d, J=2.1 Hz).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US09107916B2 |
| Source dataset | uspto-grants-2015_08 |
| ORD ID | ord-5b484bca7f1349c2b15bf3be40ab21b9 |
| Source note | uspto-grants-2015_08 |