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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 439585Generated: October 27, 2026

Formaldehyde → Diethyl P-[[[(4-methylphenyl)sulfonyl]oxy]methyl]phosphonate

https://huagongshe.com/reaction/439585

Reaction equation

Participants

RoleNameHCIDCharge
ReactantFormaldehydeHCID 712—
Reactant4-Toluenesulfonyl chlorideHCID 7397—
ReactantTriethylamineHCID 8471—
ReactantDiethylphosphiteHCID 3780918—
SolventTolueneHCID 1140—
ProductDiethyl P-[[[(4-methylphenyl)sulfonyl]oxy]methyl]phosphonateHCID 4193599—

Reaction Conditions

Temperature0 °C

Reaction Steps

A mixture of diethyl phosphite (700 g, 5.07 mmole), paraformaldehyde (190 g, 6.33 mole) and triethylamine (51.0 g, 0.50 mole) in toluene (2.8 L) is heated ca 2 hr at 85°-90° C., then under relux for ca 1 h. The resulting solution is cooled to ca. 0° C., and checked by NMR (CDCl3) for completion of the reaction (in-process control). Then p-toluenesulfonyl chloride (869 g, 4.56 mole) and triethylamine (718 g, 7.09 mole) are added with cooling (0°-10° C.). The resulting mixture is stirred at ca. 22° C. for 17-24 h and checked by NMR (CDCl3) for completion of the reaction (in-process control). The solids are removed by vacuum filtration. The filtrate is washed with water (2×) and dried over anhydrous magnesium sulfate. The solvent is evaporated in vacuo to give the title compound as an oil in 65-75% (1060-1225 g) yield. As an in-process control, NMR (CDCl3) is obtained and the product purity is assayed by HPLC C18 -35% CH3CN in KH2PO4 (0.02M)!. The purity of the product is typically 85-95%.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05514798
Source datasetuspto-grants-1996_05
ORD IDord-b80b980474044801991166c72a45aed7
Source noteuspto-grants-1996_05