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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1357768Generated: November 2, 2026

Phosphorus oxide (P4O10) → HCID 2794459, compound

https://huagongshe.com/reaction/1357768

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPhosphorus oxide (P4O10)HCID 14812—
ReactantHexamethyldisiloxaneHCID 24764—
Reactant3,5-DimethoxyanilineHCID 66301—
ReactantSodium BicarbonateHCID 516892—
ReactantTrimethyl(phosphooxy)silaneHCID 16133246—
ReactantHCID 18187381HCID 18187381—
Solvent1,2-DichloroethaneHCID 11—
ProductHCID 2794459HCID 279445916%

Reaction Steps

1.52 g (9.9 mmol) of 3,5-dimethoxyaniline and 2.30 g (12 mmol, 1.2 eq) of ethyl (α-formylphenylacetate are mixed together in a round-bottomed flask under a nitrogen atmosphere. The medium is stirred for 1 h at room temperature. A solution of trimethylsilyl polyphosphate (PPSE), freshly prepared from 4.56 g (0.03 mol) of P2O5, 10.9 ml (0.17 mol) of hexamethyldisiloxane and 50 ml of 1,2-dichloroethane, is added. The final mixture is maintained at 100° C. for 2 h. The heating is stopped and ice is then added to the reaction mixture. This mixture is then neutralized by addition of saturated sodium hydrogen carbonate solution (portionwise addition, exothermic reaction). The product is extracted with dichloromethane (large amount to be used). The organic phase is dried over MgSO4 and then evaporated under reduced pressure. The residue is taken up in ethyl acetate, which causes precipitation of the desired compound. The final product is isolated by filtration through a sinter funnel. After partial concentration of the filtrate, the final product reprecipitates. The solid is reisolated by filtration, this operation being repeated several times. Compound 34 (444 mg) is obtained in a yield of 16%.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06593342B1
Source datasetuspto-grants-2003_07
ORD IDord-f5ab0fcdffa147fc859aecee44ac17cc
Source noteuspto-grants-2003_07