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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2216139Generated: November 2, 2026

Tetraethyl methylenediphosphonate → HCID 145857658, compound

https://huagongshe.com/reaction/2216139

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTetraethyl methylenediphosphonateHCID 15455—
ReactantSodium hydrideHCID 24758—
ReactantChloroform trifluoroacetic acidHCID 19978452—
Reactanttert-butyl N-[4-[3-[2-(hydroxymethyl)-6-methylphenyl]phenyl]sulfonyl-5-methylsulfanylthiophene-2-carboximidoyl]carbamateHCID 145857676—
CatalystHCID 178418406HCID 178418406—
SolventDichloromethaneHCID 6344—
SolventTetrahydrofuranHCID 8028—
ProductHCID 145857658HCID 14585765860.8%

Reaction Steps

Manganese dioxide (0.041 g, 0.470 mmol) was added to a solution of ({[4-(2′-hydroxymethyl-6′-methyl-biphenyl-3-sulfonyl)-5-methylsulfanyl-thiophen-2-yl]-imino-methyl}-carbamic acid tert-butyl ester (0.025 g, 0.047 mmol) [example 213, step b] in dichloromethane [5 mL] and refluxed for 3 hours. The reaction was filtered through Celite and evaporated. The crude residue was dissolved in anhydrous THF [2 mL] and added to a solution of (diethoxy-phosphorylmethyl)-phosphonic acid diethyl ester (0.011 g, 0.061 mmol) and sodium hydride (0.003 g, 0.056 mmol) in THF [2 mL] at room temperature and stirred for 0.5 hours. A solution of 1N NaOH/MeOH (1/1) [10 mL] was added and the crude product was extracted with ether, dried with magnesium sulfate and evaporated. Column chromatography (50% EtOAc in hexanes) of the residue yielded the title compound (0.019 g, 57%) as a solid. ESI-MS (m/z): Calcd. for C30H37N2O7PS3: 664.15; found: 664.8.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07109354B2
Source datasetuspto-grants-2006_09
ORD IDord-11aa722c388441d0a6f050b7128305b7
Source noteuspto-grants-2006_09