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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1400778Generated: November 1, 2026

Toluene → 5'-Bromo-6-chloro-2'-fluoro-[1,1'-biphenyl]-2-ol

https://huagongshe.com/reaction/1400778

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTolueneHCID 1140—
ReactantSodium CarbonateHCID 10340—
Reactant4-Bromo-1-fluoro-2-iodobenzeneHCID 2782750—
Reactant(2-Chloro-6-hydroxyphenyl)boronic acidHCID 54758882—
CatalystHCID 178418397HCID 178418397—
SolventMethanolHCID 887—
Product5'-Bromo-6-chloro-2'-fluoro-[1,1'-biphenyl]-2-olHCID 8671083191.5%

Reaction Conditions

Temperature105 °C

Reaction Steps

(2-Chloro-6-hydroxyphenyl)boronic acid (250 mg, 1.450 mmol, 1.0 equiv), Pd(PPh3)4 (168 mg, 0.145 mmol, 0.1 equiv) and aqueous Na2CO3 (2 M, 1.8 mL, 3.63 mmol, 2.5 equiv) were mixed with toluene (3 mL) in a sealed microwave tube. 4-Bromo-1-fluoro-2-iodobenzene (436 mg, 1.450 mmol) in MeOH (1.50 mL) was added to the above mixture. The mixture was heated at 105° C. overnight. Then, the reaction mixture was loaded on 12 g column and purified using 30% EtOAc/Hex to afford 5′-bromo-6-chloro-2′-fluoro-[1,1′-biphenyl]-2-ol (400 mg, 91% yield). 1H NMR (400 MHz, CDCl3) δ 7.57 (ddd, J=8.8, 4.5, 2.5 Hz, 1H), 7.47 (dd, J=6.3, 2.5 Hz, 1H), 7.24 (t, J=8.2 Hz, 1H), 7.17-7.06 (m, 2H), 6.90 (d, J=8.0 Hz, 1H). LCMS (M+1)=302.9.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08906929B2
Source datasetuspto-grants-2014_12
ORD IDord-19daac34860a47089e1a48afd8595752
Source noteuspto-grants-2014_12