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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1198809Generated: October 30, 2026

Acetic Acid → isobutyl P-(3-cyanoprop-2-yl)-P-methyl-phosphinate

https://huagongshe.com/reaction/1198809

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetic AcidHCID 176—
ReactantSodium hydrideHCID 24758—
ReactantCrotononitrileHCID 637921—
ReactantIsobutyl methanephosphoniteHCID 86741778—
SolventEthanolHCID 702—
Productisobutyl P-(3-cyanoprop-2-yl)-P-methyl-phosphinateHCID 23374761—

Reaction Steps

A solution of 50.0 g of isobutyl P-methylphosphonite and 22.8 g of crotononitrile in 50 ml of dry ethanol is added to a stirred mixture of 0.8 g of sodium hydride (50% dispersion in oil) in 25 ml of ethanol at 0° C., under an atmosphere of nitrogen. The reaction mixture is allowed to warm to room temperature and stirred for 4 hours. 1 ml of glacial acetic acid is added and the mixture is concentrated under reduced pressure. The resulting crude product is dissolved in 50 ml of ethyl acetate, washed twice with 25 ml of water, and the organic extract is dried over magnesium sulphate, and then concentrated under reduced pressure. The crude product is distilled to give isobutyl P-(3-cyanoprop-2-yl)-P-(methyl)-phosphinate, b.p. 110°/0.125 mbar, 31P-NMR spectrum: δ=+55.9 and +55.5 ppm (CDCl3).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05281747
Source datasetuspto-grants-1994_01
ORD IDord-e675922201a246fa9265506331061ed5
Source noteuspto-grants-1994_01