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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2256889Generated: November 2, 2026

Pyridine → HCID 53666718, compound

https://huagongshe.com/reaction/2256889

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-nitro4-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-nitro4-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 numberUS05656573
Source datasetuspto-grants-1997_08
ORD IDord-dcad344b109e4af1b2c1321e6fcbe0a5
Source noteuspto-grants-1997_08