Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2225989Generated: October 31, 2026

Trimethyl borate → 4-(Methylthio)phenylboronic acid

https://huagongshe.com/reaction/2225989

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTrimethyl borateHCID 8470—
ReactantSodium HydroxideHCID 14798—
Reactant4-BromothioanisoleHCID 66037—
ReactantButyllithiumHCID 178418339—
SolventTetrahydrofuranHCID 8028—
SolventHexaneHCID 8058—
Product4-(Methylthio)phenylboronic acidHCID 273395983.3%

Reaction Steps

Under nitrogen, a stirred solution of 30 g (150 mmol) of 4-bromothioanisole (Aldrich) in 1500 mL of anhydrous THF at -78° C. was treated with 180 mmol of n-butyllithium in hexane. After 30 minutes, 51 mL (450 mmol) of trimethylborate was added neat and the reaction was allowed to warm to ambient temperature overnight. A solution of 300 mL of 10% NaOH was added and the mixture stirred vigorously for 1 h. The solvent was removed in vacuo, the pH adjusted to 4-5, and the product collected by filtration. Repeated washings with hexane and water provided 21 g (83%) of 4-methylthiophenylboronic acid (21 in Synthetic Scheme VII when R5 =SCH3 and R3, R4, R6, and R7 =H) as a colorless solid: NMR (DMSO-d6) d 2.47 (s, 3H) , 7.20 (d, J=8 Hz, 2H) , 7.71 (d, J=8 Hz, 2H) , 7.96 (br s, 2H) .

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05344991
Source datasetuspto-grants-1994_09
ORD IDord-425552bd8bfa4d7d81c2d66b6570a732
Source noteuspto-grants-1994_09