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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 266505Generated: November 1, 2026

Pyridine → HCID 53666718, compound

https://huagongshe.com/reaction/266505

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPyridineHCID 1049—
ReactantAcetyl chlorideHCID 6367—
ReactantHCID 54050151HCID 54050151—
SolventDichloromethaneHCID 6344—
ProductHCID 53666718HCID 5366671859.1%

Reaction Conditions

Temperature0 °C

Reaction Steps

A mixture of 4-[hydroxy-(2-nitro-4-trifluoromethylphenyl)-methyl]-5-cyclopropylisoxazole (0.69 g), acetyl chloride (0.27 g) and pyridine (0.10 g) in dichloromethane (40 ml) was stirred at 0° C. for 4 hours. The mixture was quenched with water and extracted with dichloromethane. The organic extracts were dried (anhydrous magnesium sulphate) and filtered. The filtrate was evaporated to dryness. The residue was triturated with ether/petroleum ether to give 4-[acetoxy-(2-nitro-4-trifluoromethylphenyl)methyl]-5-cyclopropylisoxazole (compound 297, 0.46 g) as a yellow solid: m.p. 82° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05650533
Source datasetuspto-grants-1997_07
ORD IDord-61a2e981f81540d385a97a41c1ceaf4c
Source noteuspto-grants-1997_07