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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1087641Generated: October 30, 2026

Acetic Acid → 2-(1-(3-Nitrobenzylidene)acetonyl)-2-oxo-1,3,2-dioxaphosphorinane

https://huagongshe.com/reaction/1087641

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetic AcidHCID 176—
Reactant3-NitrobenzaldehydeHCID 7449—
ReactantPiperidineHCID 8082—
Reactant2-Acetonyl-2-oxo-1,3,2-dioxaphosphorinaneHCID 13604551—
SolventWaterHCID 962—
SolventTolueneHCID 1140—
Product2-(1-(3-Nitrobenzylidene)acetonyl)-2-oxo-1,3,2-dioxaphosphorinaneHCID 5406795125.8%

Reaction Steps

A mixture of 10.0 grams of 2-acetonyl-2-oxo-1,3,2-dioxaphosphorinane and 8.48 grams of m-nitrobenzaldehyde was dissolved in 120 ml of toluene, 1.0 gram of piperidine and 2.0 grams of acetic acid were added as catalysts and the mixture was heated to reflux for 15 hours with a water-remover. After cooled, the crystals separated out were removed by filtration, the filtrate was washed with water, then with aqueous solution of sodium hydroxide, further with 20% sodium acid sulfite solution and finally with water, and the organic solvent layer was dried. The solvent was removed by evaporation in vacuo, the residue was purified by silica gel column chromatography, and 4.5 grams of 2-(1-(3-nitrobenzylidene)acetonyl)-2-oxo-1,3,2-dioxaphosphorinane was obtained as an EZ mixture. Recrystallized from ethyl acetate. M.p. 144°-145.5° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05036059
Source datasetuspto-grants-1991_07
ORD IDord-73e9e039c9eb477cbf1902f78999a98f
Source noteuspto-grants-1991_07