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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 234114Generated: October 25, 2026

Potassium Bromide → 2,5-bis(4-Bromophenyl)-3-(p-tolyloxy)furan

https://huagongshe.com/reaction/234114

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium BromideHCID 253877—
Reactant1-(4-Tolyloxy)-1,2-bis-(4-bromobenzoyl)ethyleneHCID 53957809—
SolventPhosphorus trichlorideHCID 24387—
Product2,5-bis(4-Bromophenyl)-3-(p-tolyloxy)furanHCID 10345219—

Reaction Steps

A solution of 5.0 g (0.01 mole) 1-(4-tolyloxy)-1,2-bis-(4-bromobenzoyl) ethylene in 10 ml phosphorus trichloride was heated under reflux for 3-4 hr (TLC followed). The excess PCl3 was removed by distillation and the residue was triturated with ice/water (exothermic reaction). The solution was extracted with dichloromethane (75 ml) and the dichloromethane layer was washed with saturated sodium bicarbonate solution, water, and dried (Na2SO4). The solvent was removed under reduced pressure. The residual solid was chromatographed over silica gel using ether:hexane (2:8 to 1:1) as eluant. An off white crystalline solid was obtained, 2.78 g (56%), mp 92°-3° C. IR (KBr) 2923, 2851, 1560, 1506, 1467, 1390, 1209, 1072, 1066, 945, 825, 707, 486. 1H NMR (CDCl3 /35° C.) 7.69 (d, 2H, J=8.8), 7.46-7.43 (m, 6H), 7.12 (d, 2H, J=8.3), 7.0 (d, 2H, J=8.3), 6.47 (s, 1H), 2.31 (s, 3H). 13C NMR (CDCl3 /135° C.) 150.8, 150.1, 142.8, 139.3, 133.0, 131.9, 131.7, 130.3, 129.1, 128.6, 125.1, 125.0, 121.8, 120.5, 117.1, 102.7, 20.6. MS m/e 484 (M+).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05594138
Source datasetuspto-grants-1997_01
ORD IDord-ef0126e38d014dca921edf13e5a1870f
Source noteuspto-grants-1997_01