HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1087591Generated: October 31, 2026
Potassium Carbonate → HCID 15752886, compound
https://huagongshe.com/reaction/1087591
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | Thionyl Chloride | HCID 24386 | — |
| Reactant | 2-Thiopheneglyoxylic acid | HCID 77694 | — |
| Reactant | 5-(Diethylamino)pent-3-yn-2-ol | HCID 114413 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Pyridine | HCID 1049 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 15752886 | HCID 15752886 | 30.7% |
Reaction Steps
To a solution of 4.3 g α-oxo-2-thiopheneacetic acid in dichloromethane was added 0.5 ml pyridine, and 6.75 g thionyl chloride was then added dropwise under ice cooling. The mixture was heated under reflux for seven hours and concentrated under reduced pressure, diethyl ether was added to the residue, the insoluble matters were filtered off, and the filtrate was concentrated under reduced pressure. The oily substance thus obtained (4.1 g) was added dropwise to an etheral solution of 4.5 g 5-diethylamino-3-pentyn-2-ol under ice cooling, and the mixture was stirred for 18 hours under cooling with water and basified with an aqueous solution of potassium carbonate. The separated etheral layer was collected, washed with water, dried over anhydrous magnesium sulfate and concentrated under reduced pressure. The oily residue was purified by silica gel column chromatography (Wako Gel C-200; ethyl acetate), giving 2.48 g of the objective compound as oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05036098 |
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| Source dataset | uspto-grants-1991_07 |
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| ORD ID | ord-721ca0e7c8454ee68022001a1b6aecdc |
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| Source note | uspto-grants-1991_07 |
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