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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 280035Generated: October 30, 2026

Dimethyl Sulfoxide → HCID 23323151, compound

https://huagongshe.com/reaction/280035

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDimethyl SulfoxideHCID 679—
ReactantSodium hydrideHCID 24758—
Reactant4-Chlorophenyl 2-chloro-4-nitrophenyl ketoneHCID 886296—
ReactantHCID 178418361HCID 178418361—
CatalystMethyltriphenyliphosphonium bromideHCID 74505—
SolventWaterHCID 962—
ProductHCID 23323151HCID 23323151—

Reaction Steps

To 2.5 g (0.06 mole) of 60% commercial sodium hydride was added 50 ml of sieve-dried dimethylsulfoxide. The stirring mixture was heated until evolution of hydrogen gas ceased. The mixture was cooled in an ice-box and 21.4 g (0.06 mole) of (methyl)triphenylphosphonium bromide, a Wittig reagent, dissolved in 60 ml of sieve-dried dimethylsulfoxide, was added in a few minutes. The resulting mixture was stirred for 15 minutes at room temperature. Then, 9 g (0.03 mole) of 2,4'-dichloro-4-nitrobenzophenone was added as a solid. The resulting mixture was heated at 75°-80° under nitrogen overnight. The reaction mixture was diluted with 200 ml of water and extracted with ether. The ethereal extract was dried over magnesium sulfate. The extract was evaporated to dryness. The residue was dissolved in 30 ml of methylene chloride and the solution put through a silica gel column (5.5×21 cm) with an eluant of methylene chloride/n-hexane. The selected fractions were combined and evaporated to give 2.35 g of 1-(4-chlorophenyl)-1-(2-chloro-4-nitrophenyl)ethylene.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04587361
Source datasetuspto-grants-1986_05
ORD IDord-c01132ae4b7945738ef205ab88f33d00
Source noteuspto-grants-1986_05