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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2214667Generated: November 1, 2026

2,4-Difluorobenzaldehyde → 4-Fluoro-2-(methylthio)benzaldehyde

https://huagongshe.com/reaction/2214667

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2,4-DifluorobenzaldehydeHCID 73770—
ReactantSodium methanethiolateHCID 4378561—
SolventTolueneHCID 1140—
SolventDiethyl EtherHCID 3283—
Product4-Fluoro-2-(methylthio)benzaldehydeHCID 2194740975.3%

Reaction Conditions

Temperature80 °C

Reaction Steps

A suspension of 2,4-difluorobenzaldehyde (16 mL, 146 mmol) and sodium thiomethoxide (14 g, 200 mmol) in toluene (200 mL) was stirred at 80° C. for 7 h and 14 h at room temperature. The reaction mixture was diluted with ether (300 mL), washed with water (100 mL), saturated aqueous NaHCO3 (100 mL) and brine (50 mL). The aqueous layers were combined and extracted with ether (2×100 mL). The organic layers were combined and dried over anhydrous Na2SO4, filtered and concentrated to give a viscous oil. This viscous oil was dissolved in ether/hexanes (1:1, v/v) and slowly concentrated on under vacuum. The precipitated white solid was separated by filteration and dried to give 2-methylthio-4-fluorobenzaldehyde (18.7 g, 75% yield). 1HNMR (500 MHz, CDCl3) δ: 10.11 (1H, s), 7.78 (1H, dd, J=8.55, 6.11 Hz), 6.97 (1H, dd, J=10.07, 2.44 Hz), 6.91 (1H, td, J=8.54, 2.44 Hz), 2.45 (3H, s). MS calcd for C8H7FOS (M+H): 171.2. found: 171.6.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07109186B2
Source datasetuspto-grants-2006_09
ORD IDord-468417d2d2ab4859a7e2640bd9e1ad2d
Source noteuspto-grants-2006_09