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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 745457Generated: October 31, 2026

3-Butenenitrile, 2-(acetyloxy)- → Isopentyl (3-acetoxy-3-cyanopropyl)methylphosphinate

https://huagongshe.com/reaction/745457

Reaction equation

Participants

RoleNameHCIDCharge
Reactant3-Butenenitrile, 2-(acetyloxy)-HCID 85891—
ReactantIsopentyl methanephosphoniteHCID 131714779—
ProductIsopentyl (3-acetoxy-3-cyanopropyl)methylphosphinateHCID 54245807102.3%

Reaction Conditions

Temperature72 °C

Reaction Steps

235.0 g of isopentyl methanephosphonite are heated to 72° C. under nitrogen. 0.5 g of tert.-amyl perpivalate is added to the solution, and 63.9 g of acrolein cyanohydrin acetate, in which 3.6 g of tert.-butyl pereodecanoate are dissolved, are added dropwise, with vigorous stirring at 72° C., within 2.75 hours. After reaction is complete, the mixture is stirred at 72° C. for 5 min, and 154.8 g of isopentyl methanephosphonite are distilled out. (Recovery: 94.8%). 143.8 g of 93.6% pure isopentyl (3-acetoxy-3-cyanopropyl)methylphosphinate (yield=97.9%) are obtained.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04599207
Source datasetuspto-grants-1986_07
ORD IDord-0875c69e944148a284e95bf7bdea6adb
Source noteuspto-grants-1986_07