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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1108150Generated: October 30, 2026

Sulfuryl chloride → 2-Chloro-1-[4'-[(difluoromethyl)thio][1,1'-biphenyl]-4-yl]ethanone

https://huagongshe.com/reaction/1108150

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSulfuryl chlorideHCID 24648—
Reactant2-[4'-[(Difluoromethyl)thio][1,1'-biphenyl]-4-yl]-2-methyl-1,3-dioxolaneHCID 18786432—
Solvent1,2-DichloroethaneHCID 11—
Product2-Chloro-1-[4'-[(difluoromethyl)thio][1,1'-biphenyl]-4-yl]ethanoneHCID 1878640571.6%

Reaction Steps

A solution of 8.0 g (25 mmol) of 2-[4'-[(difluoromethyl)thio][1,1'-biphenyl]-4-yl]-2-methyl-1,3-dioxolane and 30 mL of anhydrous 1,2-dichloroethane was cooled to 5° C. and sulfuryl chloride (2.3 mL, 3.8 g, 28 mmol) was added via syringe. The solution was allowed to warm to ambient temperature and concentrated to dryness. Acetone (40 mL), 5 mL of water, and 2 mL of 37% HCl were added, and the mixture was heated at 55° C. for 18 h. The mixture was diluted with 20 mL of water with cooling and seeding to precipitate the product. After filtration, washing with cold 50% aqueous MeOH and drying, the crude solid (7.2 g, 92%) was slurried in 80 mL of hot isopropanol (i-PrOH) allowed to cool with good stirring for 30 min, and filtered to afford 5.6 g of 2-chloro-1-[4'-[(difluoro-methyl)thio][1,1'-biphenyl]-4-yl]ethanone, m.p. 102-104° C. A second crop of 0.9 g was obtained by partial concentration of the filtrate. An analytical standard was prepared by chromatography and/or recrystallization from CH2Cl2 /MeOH, m.p. 104 to 105° C. 1H-NMR(CDCl3): δ4.75 (s, 2H), 6.88 (t, 1H), 7.65 (ABq, 4H) 7.7 (d, A of ABq, 2H), 8.05 (d, B of ABq, 2H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06063932
Source datasetuspto-grants-2000_05
ORD IDord-c7a7669a7ec241fb922efbff79d9966a
Source noteuspto-grants-2000_05