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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 864551Generated: November 2, 2026

Trichloromethanesulfenyl chloride → HCID 53654086, compound

https://huagongshe.com/reaction/864551

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTrichloromethanesulfenyl chlorideHCID 11666—
ReactantSodium hydrideHCID 24758—
ReactantHCID 53769132HCID 53769132—
ReactantHCID 178418361HCID 178418361—
SolventTetrahydrofuranHCID 8028—
ProductHCID 53654086HCID 5365408630%

Reaction Steps

A solution of 4-chloro-4'-trifluoromethylsulfonyloxybenzophenone-N-ethoxYcarbonylhydrazone (0.5 g) in tetrahydrofuran (6 ml) was stirred at room temperature under a nitrogen atmosphere, during which an oily mixture (50 mg) of sodium hydride containing 60% (w/w) sodium hydride was added to the solution at a time. After stirring at room temperature for 15 minutes and finding no evolution of hydrogen gas, the mixture was cooled to -78° C., and trichloromethanesulfenyl chloride (0.3 g) was added dropwise over 3 minutes. The reaction mixture was warmed to room temperature over 4 hours, and then poured into ice-water. Further, a saturated saline solution was added thereto. The aqueous layer was extracted with ethyl acetate, and the extract was combined with the organic layer. The combined organic layer was dried over anhydrous magnesium sulfate, and concentrated. The residue was subjected to silica gel chromatography, which afforded 0.2 g of 4-chloro-4'-trifluoromethylsulfonyloxybenzophenone-N-ethoxycarbonyl-N-trichloromethanesulfenylhydrazone (compound 31 ).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05563174
Source datasetuspto-grants-1996_10
ORD IDord-400b9168830042e9b1a1dde2b6516446
Source noteuspto-grants-1996_10