HuagongsheHuagongshe Chemistry Print Report · For research reference only
Water → 2-Benzyl-3-(4'-bromomethylbiphen-4-yl)benzofuran
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Water | HCID 962 | — |
| Reactant | Triphenylphosphine dibromide | HCID 70579 | — |
| Reactant | 4'-(2-Benzylbenzofuran-3-yl)biphenyl-4-methanol | HCID 68819951 | — |
| Solvent | Acetonitrile | HCID 6342 | — |
| Product | 2-Benzyl-3-(4'-bromomethylbiphen-4-yl)benzofuran | HCID 59696178 | 87% |
Reaction Steps
To a solution of 4′-(2-benzylbenzofuran-3-yl)biphenyl-4-methanol (5.01 g, 12.7 mmol) in anhydrous acetonitrile (75 mL) was added dibromtriphenylphosphorane (5.45 g, 12.7 mmol) as a solid portionwise over 15 mins. The reaction was stirred for 2 hours (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 an off-white solid (4.98 g, 87%): 1H NMR (CDCl3, 300 MHz): δ 7.70 (2H, m, Ar-H), 7.63 (4H, m, Ar-H), 7.50 (3H, m, Ar-H), 7.30 (4H, m, Ar-H), 7.25 (4H, m, Ar-H), 4.57 (2H, s, CH2Br), 4.26 (2H, PhCH2).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07524878B2 |
| Source dataset | uspto-grants-2009_04 |
| ORD ID | ord-b5cf3e8035e145d1b3f1ac2f272146b5 |
| Source note | uspto-grants-2009_04 |