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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2416593Generated: October 27, 2026

Ethanol → 4'-Methylsulfanyl-biphenyl-2-carbaldehyde

https://huagongshe.com/reaction/2416593

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthanolHCID 702—
ReactantSodium CarbonateHCID 10340—
Reactant2-BromobenzaldehydeHCID 81129—
Reactant4-(Methylthio)phenylboronic acidHCID 2733959—
SolventWaterHCID 962—
SolventTolueneHCID 1140—
Product4'-Methylsulfanyl-biphenyl-2-carbaldehydeHCID 139221796.4%

Reaction Steps

2-Bromobenzaldehyde (3.7 g, 20 mmol) and 4-(methylthio) benzeneboronic acid (3.36 g, 20 mmol) were dissolved in toluene (80 mL) and sodium carbonate (2M, 10 mL, 20 mmol) was added. To this reaction mixture was added ethanol (5 mL) followed by tetrakis (triphenylphosphine)palladium (240 mg, 0.2 mmol) and the reaction mixture was refluxed overnight under nitrogen atmosphere. The reaction mixture was cooled to room temperature and diluted with water (50 mL), stirred well, and the organic layer was separated. The aqueous layer was extracted with ethyl acetate. The combined organic layers were washed with water (2×50 mL), brine (1×50 mL), dried over sodium sulfate, filtered and the filtrate concentrated under reduced pressure to give the crude product. Purification by flash column chromatography using 5% ethyl acetate in hexane gave the title compound as a colorless thick oil (4.4 g, 96% yield). 1H NMR (CDCl3) δ9.98 (s, 1H), 8.01 (dd, J=7.8 Hz and 1.2 Hz, 1H), 7.6 (dt, J=7.5 and 1.4 Hz, 2H), 7.62-7.40 (m, 2H), 7.3-7.25 (m, 3H), 2.53 (s, 3H); LRMS (APIMS) m/z 329 (M+H)+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06825185B2
Source datasetuspto-grants-2004_11
ORD IDord-fc572af570f54c319972e994ae65d9be
Source noteuspto-grants-2004_11