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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1915875Generated: November 1, 2026

Hexachloroethane → 5-Chloro-4-nitro-1-(oxetan-3-ylmethyl)-1H-pyrazole

https://huagongshe.com/reaction/1915875

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHexachloroethaneHCID 6214—
ReactantLithium HexamethyldisilazideHCID 2733832—
Reactant4-Nitro-1-(oxetan-3-ylmethyl)pyrazoleHCID 86680079—
SolventTetrahydrofuranHCID 8028—
Product5-Chloro-4-nitro-1-(oxetan-3-ylmethyl)-1H-pyrazoleHCID 7174340995%

Reaction Conditions

Temperature-78 °C

Reaction Steps

To a solution of 4-nitro-1-(oxetan-3-ylmethyl)pyrazole (3200 mg, 17.47 mmol) in THF (80 mL) was added LHMDS (1M solution in THF, 22.7 mL, 22.7 mmol) dropwise at −78° C. over a period of 15 min. The resulting mixture was stirred at −78° C. for 30 min. Hexachloroethane (5.38 g, 22.7 mmol.) in THF (20 mL) was added at −78° C. dropwise. The resulting mixture was stirred at −78° C. for another 40 min. The reaction mixture was quenched with aqueous ammonium chloride and extracted with Ethyl acetate (×3). Combined organic layers were dried over Na2SO4 and concentrated under reduced pressure. The crude material was purified by column chromatography with 0 to 75% ethyl acetate in heptane as eluent to give 5-chloro-4-nitro-1-(oxetan-3-ylmethyl)-1H-pyrazole (3.60 g, 95%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08614206B2
Source datasetuspto-grants-2013_12
ORD IDord-a0a0abc635744ce39aac9b2e891fcf7d
Source noteuspto-grants-2013_12