HuagongsheHuagongshe Chemistry Print Report · For research reference only
Benzaldehyde → 3-Phenylprop-2-enenitrile
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Benzaldehyde | HCID 240 | — |
| Reactant | Water | HCID 962 | — |
| Reactant | Sodium hydride | HCID 24758 | — |
| Reactant | Diethyl (cyanomethyl)phosphonate | HCID 75676 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 3-Phenylprop-2-enenitrile | HCID 74667 | 69% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04990529 |
| Source dataset | uspto-grants-1991_02 |
| ORD ID | ord-cc01535135c049208ad1cfa870fee79b |
| Source note | uspto-grants-1991_02 |