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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1519341Generated: November 3, 2026

2-Chloro-5-(trifluoromethoxy)phenylboronic acid → HCID 71535531, compound

https://huagongshe.com/reaction/1519341

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-Chloro-5-(trifluoromethoxy)phenylboronic acidHCID 2763238—
ReactantMethyl 2-bromo-5-(4-(3,4-dichlorophenyl)thiazol-2-yl)benzoateHCID 86679833—
ProductHCID 71535531HCID 715355311%

Reaction Steps

Using the conditions of General Procedure A for Suzuki Coupling and Hydrolysis in Parallel Mode, 2-bromo-5-[4-(3,4-dichloro-phenyl)-thiazol-2-yl]-benzoic acid methyl ester (which may be prepared as described for Intermediate 6; 111 mg, 0.25 mmol) was reacted 2-chloro-5-(trifluoromethoxy)phenylboronic acid (available from Frontier Scientific, Inc.; 120 mg, 0.5 mmol). The resulting ester was hydrolyzed and the acid was purified to give 2′-chloro-4-[4-(3,4-dichloro-phenyl)-thiazol-2-yl]-5′-trifluoromethoxy-biphenyl-2-carboxylic acid (1.3 mg, 1%). LCMS analysis indicated that the material was ˜100% pure, as measured by UV at 214 nm.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09073881B2
Source datasetuspto-grants-2015_07
ORD IDord-35eb0abf32b845139a945e000e16c4f7
Source noteuspto-grants-2015_07