HuagongsheHuagongshe Chemistry Print Report · For research reference only
Ethanol → (3-Bromo-5-methoxyphenyl)methanol
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Ethanol | HCID 702 | — |
| Reactant | Tetrahydrofuran | HCID 8028 | — |
| Reactant | Sodium borohydride | HCID 4311764 | — |
| Reactant | 3-Bromo-5-methoxybenzaldehyde | HCID 10608698 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | (3-Bromo-5-methoxyphenyl)methanol | HCID 10608788 | 99.3% |
Reaction Steps
NaBH4 (3.85 g; WAKO) was added to an ethanol (80 mL) and THF (20 mL) mixture solution of 3-bromo-5-methoxybenzaldehyde (22 g) with ice cooling and the resulting mixture was stirred at room temperature for 3 hours. The resulting mixture was poured into ice water (300 mL) and ethyl acetate (300 mL) was added thereto to extract the mixture with and the organic layer was washed with saturated aqueous sodium bicarbonate solution (300 mL) and then dried. The solvent was evaporated under reduced pressure to give the title compound (22.05 g).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08299055B2 |
| Source dataset | uspto-grants-2012_10 |
| ORD ID | ord-d21a6e2210e746d6a1f88bff71c28453 |
| Source note | uspto-grants-2012_10 |