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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2040883Generated: October 30, 2026

Sodium hydride → HCID 57493854, compound

https://huagongshe.com/reaction/2040883

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium hydrideHCID 24758—
ReactantN-[Dimethyl(oxo)-lambda~6~-sulfanylidene]-4-methylbenzene-1-sulfonamideHCID 99226—
Reactant4-MethylenecyclohexanoneHCID 573489—
SolventDimethyl SulfoxideHCID 679—
SolventSodium ChlorideHCID 5234—
ProductHCID 57493854HCID 57493854100.2%

Reaction Steps

N-(para-Toluenesulfonyl)dimethylsulfoximine (1.49 g, 6.01 mmol) and anhydrous DMSO (5 mL) were added to NaH 60% oil dispersion (0.22 g, 5.46 mmol) kept under stirring under anhydrous inert gas atmosphere in a flamed 3 necks flask. The mixture became greenish, and then changed to yellow. After stirring at 35° C. for 10 h, a solution of 4-methylidenecylohexanone (0.2 g, 1.82 mmol) in 5 mL of DMSO was added and the reaction mixture was stirred at 50° C. for 20 h. Afterwards, the reaction mixture was diluted with a saturated solution of NaCl and extracted with Et2O (3 times). After drying on Na2SO4 and evaporation to dryness, the residue from evaporation was purified by means of automated flash chromatography (Isolera®TM-Biotage; isocratic Petroleum Ether-EtOAc 9:1) to give 0.252 g of the title compound as a colorless oil. Yield: 27.8%.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08580962B2
Source datasetuspto-grants-2013_11
ORD IDord-6d56c59f150642c2aa8ca8d02ae219bb
Source noteuspto-grants-2013_11