Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1904683Generated: October 31, 2026

Benzaldehyde → 3-Phenylprop-2-enenitrile

https://huagongshe.com/reaction/1904683

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzaldehydeHCID 240—
ReactantWaterHCID 962—
ReactantSodium hydrideHCID 24758—
ReactantDiethyl (cyanomethyl)phosphonateHCID 75676—
SolventTetrahydrofuranHCID 8028—
Product3-Phenylprop-2-enenitrileHCID 7466771.4%

Reaction Steps

Four grams of 60% sodium hydride was suspended in 100 ml tetrahydrofuran, and 17.1 g of diethylphosphonoacetonitrile was added with ice cooling. To the resulting solution, was added dropwise a solution of 10.6 g benzaldehyde in 80 ml tetrahydrofuran, and the mixture was stirred for one hour. After admixing 50 ml water, the organic layer was collected, dried over anhydrous sodium sulfate and concentrated. Distillation of the concentrate under reduced pressure (102°-106° C./6 mmHg) gave 8.9 g (yield: 69.0%) of cinnamonitrile.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04839376
Source datasetuspto-grants-1989_06
ORD IDord-48329806f4dd4281b28f26609a403720
Source noteuspto-grants-1989_06