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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 230633Generated: October 31, 2026

4-Nitrobenzyl chloride → HCID 57762790, compound

https://huagongshe.com/reaction/230633

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-Nitrobenzyl chlorideHCID 7482—
ReactantPotassium CarbonateHCID 11430—
Reactant3-(Trifluoromethyl)-4,5,6,7-tetrahydro-1H-indazoleHCID 2802863—
SolventDimethylformamideHCID 6228—
ProductHCID 57762790HCID 57762790115.4%

Reaction Steps

A solution of 3-(trifluoromethyl)-4,5,6,7-tetrahydro-1H-indazole (380 mg, 2 mmol) in anhydrous DMF (10 ml) was treated with potassium carbonate (552 mg, 4 mmol) followed by 4-nitrobenzyl chloride (343 mg, 2 mmol) and the whole mix stirred under argon for 16 h at room temperature. The reaction mixture was separated between water (20 ml) and ethyl acetate (20 ml). The organic layer was washed again with a water/brine mix (1:1) (10 ml) then dried over sodium sulphate and the solvent removed under reduced pressure to give a yellow oil (751 mg) which was chromatographed on a 5 g pre-packed silica column eluting from 0-20% ethyl acetate in petroleum ether to give the title compound as a yellow oil (416 mg, 64%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07566735B2
Source datasetuspto-grants-2009_07
ORD IDord-1261e051e3024110b7801f4539c1e106
Source noteuspto-grants-2009_07