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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1438129Generated: October 31, 2026

Trimethyl borate → (4-Chloro-3-methoxyphenyl)boronic acid

https://huagongshe.com/reaction/1438129

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTrimethyl borateHCID 8470—
Reactant5-Bromo-2-chloroanisoleHCID 2769567—
ReactantButyllithiumHCID 178418339—
SolventTetrahydrofuran tolueneHCID 22635083—
Product(4-Chloro-3-methoxyphenyl)boronic acidHCID 2300537765%

Reaction Conditions

Temperature-78 °C

Reaction Steps

To 4-bromo-1-chloro-2-methoxybenzene (2.2 g, 9.9 mmol) in toluene/THF (16/6 mL) at −78° C. was added n-butyl lithium (8.7 mL, 1.6 M in hexane, 14 mmol) dropwise. The reaction was stirred at −78° C. for 30 min, then trimethylborate (2.2 mL, 19.8 mmol) was added. The reaction was allowed to warm to rt and stirred overnight and then quenched with 1 M HCl (15 mL). The organic layer was separated and dried over sodium sulfate. The solvent was removed and the crude product was purified by flash column chromatography to give 50A (1.2 g, 65% yield) as a white solid. 1H NMR (400 MHz, Methanol-d4) δ ppm 3.87 (m, 3H) 7.11 (d, J=7.83 Hz, 1H) 7.20 (s, 1H) 7.29 (d, J=7.83 Hz, 1H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07622585B2
Source datasetuspto-grants-2009_11
ORD IDord-f638a123cd6e4555abeea52df9a04b37
Source noteuspto-grants-2009_11