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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1939421Generated: October 29, 2026

Trimethyl borate → 5-Chloro-2-methoxyphenylboronic acid

https://huagongshe.com/reaction/1939421

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTrimethyl borateHCID 8470—
Reactant2-Bromo-4-chloroanisoleHCID 521935—
Reactant5-Fluoro-2-methoxyphenylboronic acidHCID 2782673—
ReactantButyllithiumHCID 178418339—
Product5-Chloro-2-methoxyphenylboronic acidHCID 273575177%

Reaction Steps

This compound was prepared in a manner similar to that of 5-fluoro-2-methoxyphenylboronic acid (EXAMPLE 107) from 2-bromo-4-chloroanisole (2.00 g, 9.01 mmol, 1.0 equivuiv), n-BuLi (2.5M in hexanes; 3.62 mL, 9.01 mmol, 1.0 equivuiv), and trimethylborate (3.0 mL, 26 mmol, 2.9 equivuiv) to afford 1.30 g (77%) of crude 5-chloro-2-methoxyphenylboronic acid as a white semi-solid. This compound was used in the next reaction with no further purification.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05696127
Source datasetuspto-grants-1997_12
ORD IDord-ddc851fcca2f455d89a403a28db837a7
Source noteuspto-grants-1997_12