HuagongsheHuagongshe Chemistry Print Report · For research reference only
Pyridine → 4-n-Pentylphenyl 5-n-pentyl-thieno[3,2-b]thiophene-2-carboxylate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Pyridine | HCID 1049 | — |
| Reactant | 4-Pentylphenol | HCID 26975 | — |
| Reactant | 5-n-Pentyl-thieno[3,2-b]thiophene-2-carboxylic acid chloride | HCID 56633522 | — |
| Solvent | Toluene | HCID 1140 | — |
| Product | 4-n-Pentylphenyl 5-n-pentyl-thieno[3,2-b]thiophene-2-carboxylate | HCID 20220456 | — |
Reaction Steps
3.5 g of 5-n-pentyl-thieno[3,2-b]thiophene-2-carboxylic acid chloride [obtainable by reacting 5-n-pentylthieno[3,2-b]thiophene-5-carboxylic acid (m.p. 156°, c.p. 196°) with thionyl chloride] in 20 ml of toluene are added dropwise to a mixture of 2.25 g of 4-n-pentylphenol, 1.08 g of pyridine and 30 ml of toluene, the mixture is heated to the boil for 2 hours and allowed to cool, the pyridine hydrochloride is filtered off, and the mixture is worked up in the usual manner. 4-n-Pentylphenyl 5-n-pentyl-thieno[3,2-b]thiophene-2-carboxylate of melting point 58° and clear point 93° is obtained.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04639328 |
| Source dataset | uspto-grants-1987_01 |
| ORD ID | ord-0ab4f1dadaa140caa50d46a4b95cd1a8 |
| Source note | uspto-grants-1987_01 |