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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1722633Generated: November 1, 2026

Benzenesulfonyl chloride → HCID 53933859, compound

https://huagongshe.com/reaction/1722633

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzenesulfonyl chlorideHCID 7369—
ReactantTetraethyl aminomethylenediphosphonateHCID 2773808—
Catalyst4-(Dimethylamino)pyridineHCID 14284—
SolventPyridineHCID 1049—
SolventEthyl AcetateHCID 8857—
ProductHCID 53933859HCID 53933859—

Reaction Steps

To a solution of tetraethyl (aminomethylene)bis(phosphonate) (661 mg) in pyridine (2 ml) were added benzenesulfonyl chloride (0.35 ml) and then 4-(dimethylamino)pyridine (50 mg) at ambient temperature with stirring. After stirring for 4 hours at the same temperature, the reaction mixture was diluted with ethyl acetate (20 ml). The mixture was washed with 1N hydrochloric acid four times, water and saturated aqueous hydrogen bicarbonate solution successively. The organic layer was dried over magnesium sulfate and evaporated under reduced pressure. The residue was subjected to column chromatography on silica gel (20 g) eluted with a mixture of chloroform and methanol (20:1 V/V) to give tetraethyl (phenylsulfonylaminomethylene)bis(phosphonate) as a yellow syrup (364 mg).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04857513
Source datasetuspto-grants-1989_08
ORD IDord-bdf8183fc77c4ab8ba7a1de68ad11673
Source noteuspto-grants-1989_08