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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 423697Generated: October 29, 2026

Pentane → 2-Methyl-4-methylthiophenylboronic acid

https://huagongshe.com/reaction/423697

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPentaneHCID 8003—
ReactantTrimethyl borateHCID 8470—
Reactant(4-Bromo-3-methylphenyl)(methyl)sulfaneHCID 26370189—
ReactantHCID 178418306HCID 178418306—
SolventDiethyl EtherHCID 3283—
Product2-Methyl-4-methylthiophenylboronic acidHCID 2259129850%

Reaction Conditions

Temperature-78 °C

Reaction Steps

1.7M tert-Butyllithium in pentane (6.70 mL, 11.39 mmol) was added dropwise to a solution of 1-bromo-2-methyl-4-(methylthio)benzene (1.2 g, 5.53 mmol) in diethyl ether (120 mL) at −78° C. over 15 min. The mixture was stirred at −78° C. for 2 min, then charged with trimethyl borate (0.661 mL, 5.91 mmol) dropwise over 2 min at −78° C., stirred at −78° C. for 15 min, then brought to ambient temperature. The mixture was quenched with saturated aqueous NH4Cl (14 mL), stirred at ambient temperature for 15 min, charged with 1M HCl (12 mL), stirred at ambient temperature for 2 min, and the organics were separated. The organics were dried over MgSO4, filtered, and the filtrate was concentrated. The crude product was purified by chromatography on a silica gel column using 20 to 100% EtOAc/hexane to give 503 mg (50%) of [2-methyl-4-(methylthio)phenyl]boronic acid as a white solid. 1H NMR (400 MHz, DMSO-d6): δ 7.79 (d, 1H, J=7.8 Hz), 7.09-7.00 (m, 2H), 2.61 (s, 3H), 2.46 (s, 3H); LRMS (ESI), m/z 183 (M+H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08101634B2
Source datasetuspto-grants-2012_01
ORD IDord-0763221d05e04016892eae0868bd4ba3
Source noteuspto-grants-2012_01