HuagongsheHuagongshe Chemistry Print Report · For research reference only
2-Thiophenecarboxaldehyde → HCID 21435162, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 2-Thiophenecarboxaldehyde | HCID 7364 | — |
| Reactant | Sodium Methoxide | HCID 10942334 | — |
| Reactant | HCID 54217811 | HCID 54217811 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | HCID 21435162 | HCID 21435162 | — |
Reaction Steps
A solution of 73.0 g of 2-thiophenaldehyde and 170 g of diethyl-1-(o-cyanophenyl)ethylphosphonate in 800 ml of anhydrous dimethyl formamide was added dropwise in a nitrogen atmosphere at 20°-30°to a suspension of 39.0 g of sodium methylate in 500 ml of anhydrous dimethyl formamide. The mixture was further stirred for 1 hour at 40°, cooled to 10°-15° and treated with ca. 5 1 of icewater. Working up gave 2-[1-(2-thienyl)-2-propenyl]benzonitrile, B.Pt. (0.1 to 0.2 mm Hg) = 200°-210° .
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04024266 |
| Source dataset | uspto-grants-1977_05 |
| ORD ID | ord-184f72439db5471d8efec10845114af0 |
| Source note | uspto-grants-1977_05 |