HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1478191Generated: October 31, 2026
Acetaldehyde → Ethyl 4-methyl-5-(6-methyl-3,6-dihydro-2H-pyran-2-yl)isoxazole-3-carboxylate
https://huagongshe.com/reaction/1478191
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Acetaldehyde | HCID 177 | — |
| Reactant | Ammonium Chloride | HCID 25517 | — |
| Reactant | Trimethylsilyl triflate | HCID 65367 | — |
| Reactant | Ethyl 5-(1-hydroxybut-3-en-1-yl)-4-methylisoxazole-3-carboxylate | HCID 118511124 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | Ethyl 4-methyl-5-(6-methyl-3,6-dihydro-2H-pyran-2-yl)isoxazole-3-carboxylate | HCID 118511051 | — |
Reaction Steps
A solution of ethyl 5-(1-hydroxybut-3-en-1-yl)-4-methylisoxazole-3-carboxylate (35 mg, 0.155 mmol) in DCM (1 mL) was treated with acetaldehyde (8.72 μl, 0.155 mmol) and the reaction mixture was cooled to 0° C. A solution of TMSOTf (80.4 μL, 0.465 mmol) in DCM (1.5 mL) cooled to 0° C. was added and the reaction mixture was stirred at 0° C. for 30 minutes and at room temperature overnight. To the resulting mixture was added a saturated solution of ammonium chloride (aq) (2 mL) and this was extracted with DCM (×3). The combined organic extracts were passed through a phase separating cartridge and the eluent was concentrated under reduced pressure. The crude material was adsorbed onto silica and purification by chromatography eluting with 0-100% EtOAc in iso-hexane afforded the title compound;
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09403810B2 |
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| Source dataset | uspto-grants-2016_08 |
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| ORD ID | ord-340c3bd3c0644439af908797ab392bf6 |
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| Source note | uspto-grants-2016_08 |
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