Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 864550Generated: October 30, 2026

Sodium hydride → HCID 131719604, compound

https://huagongshe.com/reaction/864550

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium hydrideHCID 24758—
ReactantHCID 54408928HCID 54408928—
ReactantHCID 131719603HCID 131719603—
ReactantHCID 178418361HCID 178418361—
SolventTetrahydrofuranHCID 8028—
ProductHCID 131719604HCID 13171960445.6%

Reaction Steps

A solution of 4-chloro-4'-trifluoromethylsulfonyloxybenzophenone-N-acetylhydrazone (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 chloro-{N-(2-ethoxycarbonylethyl)-N-isopropylamino}sulfide (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-ac etyl -N- {N '-(2-ethoxycarbonylethyl)-N'-isopropylaminosulfenyl}hydrazone (compound 24).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05563174
Source datasetuspto-grants-1996_10
ORD IDord-45ce8612137c48b49da82d6639c14eb3
Source noteuspto-grants-1996_10