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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 342952Generated: October 30, 2026

Pyridine → HCID 53666718, compound

https://huagongshe.com/reaction/342952

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 numberUS05859283
Source datasetuspto-grants-1999_01
ORD IDord-cbdaa42eeff54f8b88972f2327315a40
Source noteuspto-grants-1999_01