HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1708973Generated: October 25, 2026
Triethylamine → 1-(2-Thienyl)propyl isocyanide
https://huagongshe.com/reaction/1708973
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | Phosphorus oxychloride | HCID 24813 | — |
| Reactant | 2-(1-Formylaminopropyl) thiophene | HCID 14835444 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | 1-(2-Thienyl)propyl isocyanide | HCID 15288588 | 86.4% |
Reaction Steps
231 g of triethylamine are added to a solution of 96.5 g of 2-(1-formylaminopropyl) thiophene in 500 ml of methylene chloride and the mixture is cooled at below -30° C. 105 g of phosphorus oxychloride are added dropwise to the mixture at below -30° to -20° C. and and the mixture is stirred at the same temperature for 1 hour. After the reaction, the mixture is poured into 1 litter of an aqueous 10% potassium carbonate solution. The aqueous mixture is stirred at room temperature for 1 hour and the methylene chloride layer is separated therefrom. Said methylene chloride layer is washed with water, dried and evaporated to remove solvent. The residue is distilled under reduced pressure to give 74.5 g of 1-(2-thienyl)propyl isocyanide as a colorless oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04946862 |
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| Source dataset | uspto-grants-1990_08 |
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| ORD ID | ord-be998bdbb08141de8764b58e892ed2c4 |
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| Source note | uspto-grants-1990_08 |
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