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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 274206Generated: October 30, 2026

Triethylamine → HCID 15107320, compound

https://huagongshe.com/reaction/274206

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
ReactantButyryl chlorideHCID 8855—
ReactantHCID 15107319HCID 15107319—
SolventTetrahydrofuranHCID 8028—
ProductHCID 15107320HCID 1510732035.5%

Reaction Conditions

Temperature0 °C

Reaction Steps

12.6 g of triethylamine was added to 27.9 g of 6-(3-isopropylisoxazol-5-yl)-tetrahydropyran-2,4-dione in 200 ml of THF. At 0° C., 13.3 g of butyryl chloride was dripped in and the mixture was stirred for one hour at 0° C. The mixture was evaporated, followed by partitioning between methylene chloride and water. The organic phase was worked up, i.e., extracted with water, 10% strength sodium carbonate solution and again with water, dried with sodium sulfate and evaporated again. The residue was dissolved in anhydrous methylene chloride and stirred for 48 hours with 1.3 g of 4-(N,N-dimethylamino)-pyridine. Removal of the solvent was followed by chromatography over silica gel with methylene chloride and methanol (98.5:1.5). The isolated compound was recrystallized from a small amount of cyclohexane. There was obtained 13 g of product.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05389602
Source datasetuspto-grants-1995_02
ORD IDord-e42882b0d17a49878d31e8a95fd34d0f
Source noteuspto-grants-1995_02