HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 629127Generated: October 31, 2026
Butyryl chloride → HCID 118228953, compound
https://huagongshe.com/reaction/629127
Participants
| Role | Name | HCID | Charge |
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| Reactant | Butyryl chloride | HCID 8855 | — |
| Reactant | 6-Ethyl-4-hydroxy-2H-pyran-2-one | HCID 54713558 | — |
| Solvent | Trifluoroacetic acid | HCID 6422 | — |
| Product | HCID 118228953 | HCID 118228953 | 65% |
Reaction Steps
According to the method of Douglas and Money (see: Can. J. Chem. 1968, 46, 695), 4-hydroxy-6-ethyl-2-pyrone (see: Hsung, et. al. Synthesis 2007, 749; 1.24 g, 8.85 mmol) was dissolved in trifluoroacetic acid (4 mL) in a pressure-safe vessel. Butyryl chloride (1.0 mL, 9.73 mmol) was added and the solution flushed with argon. The vessel was sealed and stirred in a 90° C. heating bath overnight. After cooling to room temperature, the solution was poured onto powdered sodium bicarbonate (9 g) before water (80 mL) was added carefully. Organics were extracted from the aqueous slurry with dichloromethane (3×80 mL), dried with magnesium sulfate, filtered, and concentrated. The crude product was purified by chromatography on silica gel with gradient elution (10→20% ether in hexanes) to afford 3-butyryl-6-ethyl-4-hydroxy-2-pyrone (1.20 g, 65%) as an oily solid. Used without further characterization.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09315495B2 |
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| Source dataset | uspto-grants-2016_04 |
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| ORD ID | ord-035e07a7f0db46889748e5f7de6bcacd |
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| Source note | uspto-grants-2016_04 |
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