HuagongsheHuagongshe Chemistry Print Report · For research reference only
Water → 4'-(2-Benzylbenzofuran-3-yl)biphenyl-4-methanol
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Water | HCID 962 | — |
| Reactant | Sodium borohydride | HCID 4311764 | — |
| Reactant | 4'-(2-Benzylbenzofuran-3-yl)biphenyl-4-carbaldehyde | HCID 59855511 | — |
| Solvent | Ethanol | HCID 702 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 4'-(2-Benzylbenzofuran-3-yl)biphenyl-4-methanol | HCID 68819951 | 99.7% |
Reaction Steps
To a solution of 4′-(2-benzylbenzofuran-3-yl)biphenyl-4-carbaldehyde (5.0 g, 12.9 mmol) in ethanol (100 mL) and tetrahydrofuran (25 mL) was added sodium borohydride (980 mg, 25.8 mmol) as a solid in 3 portions. The reaction was stirred at room temperature for 1 hour (TLC control) and then poured into water (100 mL) and extracted with diethyl ether (3×100 mL). The combined extract was washed with water, brine, dried over anhydrous MgSO4, filtered and concentrated in vacuo to afford the title compound as a white solid (5.02 g, 99%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07524878B2 |
| Source dataset | uspto-grants-2009_04 |
| ORD ID | ord-847cf8162f654f989573b33233f75225 |
| Source note | uspto-grants-2009_04 |