HuagongsheHuagongshe Chemistry Print Report · For research reference only
3-Bromobenzoic acid → 3-Bromobenzyl alcohol
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 3-Bromobenzoic acid | HCID 11456 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 3-Bromobenzyl alcohol | HCID 85141 | — |
Reaction Steps
To a solution of 50.0 g (0.25 mols, Aldrich) of 3-bromobenzoic acid in 100 ml of dry tetrahydrofuran (THF) cooled to 0° is added slowly 100 ml (1.0M in THF, 100 mmols, Aldrich) of borane-tetrahydrofuran complex. The reaction is stirred at 0° for 1 hour then at room temperature for 18 hours. The reaction is quenched by dropwise addition of water then concentrated in vacuo to remove solvent. The residue is partitioned between diethyl ether and 1M aqueous HCl. The organic layer is separated, washed with 1M aqueous sodium hydroxide, brine, dried (magnesium sulfate) and concentrated in vacuo to afford title compound.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05153327 |
| Source dataset | uspto-grants-1992_10 |
| ORD ID | ord-52210bfb74a542e19ea8b7fd8f2c9e76 |
| Source note | uspto-grants-1992_10 |