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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

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetaldehydeHCID 177—
ReactantAmmonium ChlorideHCID 25517—
ReactantTrimethylsilyl triflateHCID 65367—
ReactantEthyl 5-(1-hydroxybut-3-en-1-yl)-4-methylisoxazole-3-carboxylateHCID 118511124—
SolventDichloromethaneHCID 6344—
ProductEthyl 4-methyl-5-(6-methyl-3,6-dihydro-2H-pyran-2-yl)isoxazole-3-carboxylateHCID 118511051—

Reaction Conditions

Temperature0 °C

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09403810B2
Source datasetuspto-grants-2016_08
ORD IDord-340c3bd3c0644439af908797ab392bf6
Source noteuspto-grants-2016_08