Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 572622Generated: October 31, 2026

Dimethyl Sulfoxide → HCID 12451263, compound

https://huagongshe.com/reaction/572622

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDimethyl SulfoxideHCID 679—
ReactantMethyl iodideHCID 6328—
ReactantCarbon DisulfideHCID 6348—
ReactantSodium hydrideHCID 24758—
Reactant3-(3,4-Dichlorophenyl)-3-oxopropanenitrileHCID 2758063—
SolventWaterHCID 962—
ProductHCID 12451263HCID 1245126359%

Reaction Steps

To a solution of 3-(3,4-dichlorophenyl)-3-oxopropanenitrile (3.3 g, 15.4 mmol) and carbon disulfide (0.927 mL, 15.4 mmol) in DMSO (50 mL) under an atmosphere of argon at 15° C. was added sodium hydride (0.856 g, 033.9 mmol) with vigorous stirring. The reaction mixture was stirred at this temperature for 10 min and was allowed to warm to rt. To the reaction mixture was added methyl iodide (1.92 mL, 30.8 mmol) and the mixture was stirred at rt for 30 min. The reaction mixture was diluted with water and extracted with EtOAc. The organic solutions were combined, washed with brine, dried over MgSO4, filtered and concentrated. The crude product was purified by column chromatography to give 2-(3,4-dichlorobenzoyl)-3,3-bis(methylsulfanyl)acrylonitrile (2.9 g, 59%). LCMS: (FA) ES-318.1. 1H NMR (400 MHz, CDCl3) δ: 7.95 (d, 1H), 7.73 (dd, 1H), 7.56 (d, 1H), 2.82 (s, 3H) and 2.55 (s, 3H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09029411B2
Source datasetuspto-grants-2015_05
ORD IDord-f077281237ad4d9c910411a628761627
Source noteuspto-grants-2015_05