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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1043429Generated: October 30, 2026

1,3-Dibromobenzene → 3-Bromo-3'-vinylbiphenyl

https://huagongshe.com/reaction/1043429

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1,3-DibromobenzeneHCID 7927—
ReactantPotassium CarbonateHCID 11430—
Reactant3-Vinylphenylboronic Acid (contains varying amounts of Anhydride)HCID 4366886—
SolventWaterHCID 962—
Solvent1,2-DimethoxyethaneHCID 8071—
Product3-Bromo-3'-vinylbiphenylHCID 5926657060%

Reaction Conditions

Temperature80 °C

Reaction Steps

A solution of 1,3-dibromobenzene (5.3 mL, 43.9 mmol), potassium carbonate (14.0 g, 101 mmol) and 3-vinylphenylboronic acid (5 g, 33.8 mmol) in DME (100 mL) and water (20 mL) (in a pressure vessel) was sparged with nitrogen for 15 min. Pd(PPh3)3 (1.17 g, 1.014 mmol) was added and then the reaction was heated to 80° C. overnight. The reaction was cooled to r.t. and evaporated on the rotovap. The residue was diluted in EtOAc and washed with water then brine, dried over MgSO4, filtered and evaporated to give the crude material. The crude material was purified by flash chromatography on the Biotage (0-5% EtOAc:Hex) to give 3-bromo-3′-vinylbiphenyl (5.21 g, 20.10 mmol, 60% yield) as a clear liquid. 1H NMR (400 MHz, CHLOROFORM-d) δ ppm 5.33 (d, J=10.79 Hz, 1H) 5.84 (dd, J=17.57, 0.75 Hz, 1H) 6.80 (dd, J=17.57, 10.79 Hz, 1H) 7.32 (t, J=7.78 Hz, 1H) 7.38-7.48 (m, 3H) 7.51 (dddd, J=13.24, 7.84, 1.76, 1.00 Hz, 2H) 7.56-7.61 (m, 1H) 7.76 (t, J=1.88 Hz, 1H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08563505B2
Source datasetuspto-grants-2013_10
ORD IDord-ccae06a7d45b488fb54190fb3a1e0423
Source noteuspto-grants-2013_10