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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1485599Generated: October 26, 2026

2-Chloro-6-fluoroanisole → HCID 178506719, compound

https://huagongshe.com/reaction/1485599

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-Chloro-6-fluoroanisoleHCID 2773581—
Reactant2-(4-Chloro-2-fluoro-3-methoxyphenyl)-4,4,5,5-tetramethyl-1,3,2-dioxaborolaneHCID 67017493—
ReactantButyllithiumHCID 178418339—
ProductHCID 178506719HCID 178506719—

Reaction Steps

Another embodiment of the present disclosure includes a method of forming 2-(4-chloro-2-fluro-3-methoxylphenyl)-4,4,5,5-tetramethyl-1,3,2-dioxaborolane that comprises contacting 2-chloro-6-fluoroanisole with n-butyl lithium to form 6-chloro-2-fluoro-3-lithioanisole. The 6-chloro-2-fluoro-3-lithioanisole may be contacted with trimethyl borate to form dimethyl 4-chloro-2-fluoro-3-methoxyphenylboronate. The dimethyl 4-chloro-2-fluoro-3-methoxyphenylboronate may be reacted with aqueous potassium hydroxide to form potassium (4-chloro-2-fluoro-3-methoxyphenyl)trihydroxyborate. The potassium (4-chloro-2-fluoro-3-methoxyphenyl)trihydroxyborate then may be reacted with aqueous hydrochloric acid to form 4-chloro-2-fluoro-3-methoxyphenylboronic acid. The 4-chloro-2-fluoro-3-methoxyphenylboronic acid may be reacted with 2,3-dimethyl-2,3-butanediol.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09422313B2
Source datasetuspto-grants-2016_08
ORD IDord-243ca6e13ce5452da27471bc22a9dffd
Source noteuspto-grants-2016_08