HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1679770Generated: October 30, 2026
Toluene → (Pyridin-2-yl)(thiophen-2-yl)acetonitrile
https://huagongshe.com/reaction/1679770
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Toluene | HCID 1140 | — |
| Reactant | 2-Chloropyridine | HCID 7977 | — |
| Reactant | Sodium amide | HCID 24533 | — |
| Reactant | 2-Thienylacetonitrile | HCID 72880 | — |
| Solvent | Water | HCID 962 | — |
| Product | (Pyridin-2-yl)(thiophen-2-yl)acetonitrile | HCID 14337913 | — |
Reaction Steps
To a well-stirred solution containing 61.5 g. of 2-thienylacetonitrile and 56.5 g. of 2-chloropyridine in 400 ml. of toluene, slowly add a stirred suspension of 40 g. of sodamide in 300 ml. of toluene keeping the reaction temperature at 60°-65° C by cooling with an ice bath. After completing the addition maintain the temperature at 60° C for 2 hrs., add 200 ml. of water to the cooled reaction mixture, decant the tarry by-products and separate the aqueous layer. Evaporate in vacuo the resulting solution and dilute the thick black residue with 300 ml. of ether. Filter the separated solid and evaporate the filtrate. The desired product is distilled off at 145°-150° C/1 ml. and is recrystallized from alcohol to yield α-(2-thienyl)-2-pyridylacetonitrile, m.p. 48°-50° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US04081544 |
|---|
| Source dataset | uspto-grants-1978_03 |
|---|
| ORD ID | ord-a47b637acb114e378a2f5e40e5097bfd |
|---|
| Source note | uspto-grants-1978_03 |
|---|