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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1632027Generated: October 31, 2026

Toluene → (3'-Chloro-2-fluoro-6-methoxy-biphenyl-3-yl)-methanol

https://huagongshe.com/reaction/1632027

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTolueneHCID 1140—
ReactantSodium CarbonateHCID 10340—
Reactant(3-Chlorophenyl)boronic acidHCID 2734323—
Reactant(3-Bromo-2-fluoro-4-methoxyphenyl)methanolHCID 57703782—
CatalystHCID 178418397HCID 178418397—
SolventEthanolHCID 702—
Product(3'-Chloro-2-fluoro-6-methoxy-biphenyl-3-yl)-methanolHCID 5770378874.1%

Reaction Conditions

Temperature80 °C

Reaction Steps

Into a 100 mL round bottom flask was added (3-bromo-2-fluoro-4-methoxy-phenyl)-methanol (I-31, 1.04 g, 4.0 mmol), 3-chlorophenylboronic acid (0.76 g, 4.8 mmol), Pd(PPh3)4 (0.45 g, 0.41 mmol), Na2CO3 (6 mL, 2M aq), toluene, (32 mL), and EtOH (11 mL). The reaction was degassed with N2, then stirred at 80° C. for 24 hours. Water was added and the product was extracted with ethyl acetate. The combined organics were concentrated and filtered through a SiO2 plug eluting with 50% ethyl acetate/hexanes. The solid was triturated with ether and filtered. The filtrate was concentrated and triturated with ether and filtered. The filter cakes were combined and purified by flash column chromatography eluting with 20% acetone/hexanes to give (3′-chloro-2-fluoro-6-methoxy-biphenyl-3-yl)-methanol (I-32, 0.79 g, 67%) as a white solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08791267B2
Source datasetuspto-grants-2014_07
ORD IDord-005c295a104b456bba38f83387c612e3
Source noteuspto-grants-2014_07