HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1200053Generated: November 2, 2026
Pyridine → 3-[2-(5-Acetoxymethyl-2-thienyl)ethenyl]benzo[b]thiophene
https://huagongshe.com/reaction/1200053
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Pyridine | HCID 1049 | — |
| Reactant | Acetyl chloride | HCID 6367 | — |
| Reactant | HCID 54225068 | HCID 54225068 | — |
| Solvent | Water | HCID 962 | — |
| Product | 3-[2-(5-Acetoxymethyl-2-thienyl)ethenyl]benzo[b]thiophene | HCID 54240120 | 51.1% |
Reaction Steps
To a stirred solution of 3-[2-(5-hydroxymethyl-2-thienyl)ethenyl]-benzo[b]thiophene (5.35 g) and pyridine (50 ml) was added over 5 mins acetyl chloride (1.54 g). The mixture was stirred at ambient temperature overnight and was poured into water (500 ml). The mixture was extracted with dichlormethane, and the combined organic phase was washed with 5% aqueous hydrochloric acid, dried over anhydrous sodium sulfate, filtered, and concentrated. The residue was purified by high performance liquid chromatography (silica gel, sample loaded in dichloromethane, eluted with 15% ethyl acetate in hexane.) The appropriate fractions were combined and concentrated. The residue was recrystallized from cyclohexane to afford 3.15 g (51%) of product, mp 66°-68° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US04904674 |
|---|
| Source dataset | uspto-grants-1990_02 |
|---|
| ORD ID | ord-08892ef21dd746ccb6f8ceb03f86a93e |
|---|
| Source note | uspto-grants-1990_02 |
|---|