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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1887184Generated: November 1, 2026

Hydrochloric Acid → 2-Propionylpent-4-enenitrile

https://huagongshe.com/reaction/1887184

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantEthyl PropionateHCID 7749—
ReactantPent-2-enenitrileHCID 25833—
ReactantPotassium tert-butoxideHCID 23665647—
SolventWaterHCID 962—
SolventO-XyleneHCID 7237—
SolventTetrahydrofuranHCID 8028—
Product2-Propionylpent-4-enenitrileHCID 8664123892.3%

Reaction Conditions

Temperature48 °C

Reaction Steps

In a 20 l jacketed reactor fitted with heating/cooling circuit and reflux condenser, 3500 g of potassium tert-butoxide were initially charged, and 6316 g of tetrahydrofuran was added. At a temperature of at most 10° C., a mixture of 1200 g of pentenenitrile and 1651 g of ethyl propionate was then pumped in over a period of 75 min. Stirring was continued at 8 to 10° C. for 3 h and then at 15° C. overnight. The mixture was then adjusted to pH of 3.8 by pumping in 6316 g of 20% strength hydrochloric acid, with the temperature increasing to 48° C. 2400 ml of water and 4000 ml of o-xylene were then added. The aqueous (lower) phase was then removed, and the organic phase was washed two more times with in each case 2400 ml of water. What remained were 14650 g of organic phase. Concentration on a rotary evaporator at 60° C. and 10 mbar gave 1873 g of an amber product having a content of 87.4% a/a (GC), which was reacted further as such.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08501748B2
Source datasetuspto-grants-2013_08
ORD IDord-dc796334b4174490be9ce9b36df3b715
Source noteuspto-grants-2013_08