HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1722633Generated: November 1, 2026
Benzenesulfonyl chloride → HCID 53933859, compound
https://huagongshe.com/reaction/1722633
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Benzenesulfonyl chloride | HCID 7369 | — |
| Reactant | Tetraethyl aminomethylenediphosphonate | HCID 2773808 | — |
| Catalyst | 4-(Dimethylamino)pyridine | HCID 14284 | — |
| Solvent | Pyridine | HCID 1049 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | HCID 53933859 | HCID 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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04857513 |
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| Source dataset | uspto-grants-1989_08 |
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| ORD ID | ord-bdf8183fc77c4ab8ba7a1de68ad11673 |
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| Source note | uspto-grants-1989_08 |
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