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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 490564Generated: October 30, 2026

Hydrochloric Acid → 6-Chloro-1-(2-chloro-benzyl)-5-nitro-1,2-dihydro-indazol-3-one

https://huagongshe.com/reaction/490564

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantPotassium CarbonateHCID 11430—
Reactantalpha-Bromo-o-chlorotolueneHCID 11905—
ReactantHCID 86604125HCID 86604125—
SolventWaterHCID 962—
Product6-Chloro-1-(2-chloro-benzyl)-5-nitro-1,2-dihydro-indazol-3-oneHCID 68831736—

Reaction Conditions

Temperature50 °C

Reaction Steps

Chloro-5-nitro-1,2-dihydro-indazol-3-one (prepared in analogy to Org. Synth. 1949, 29, 54 or Chem Ber. 1942, 75, 1104 from 4-chloro-2-fluoro-5-nitro-benzoic acid over two steps) (0.6 g) was suspended in water (5 mL) and 2N K2CO3 (aq.) (1 g) was added to the flask and the mixture was heated to 50° C. for 10 minutes. 2-Chlorobenzylbromide (0.40 g) was then added dropwise. The reaction was stirred overnight and was neutralized with 2 N HCl (aq.) while cooling in an ice bath. The precipitate was collected by filtration and triturated with diethylether to afford pure desired 6-chloro-1-(2-chloro-benzyl)-5-nitro-1,2-dihydro-indazol-3-one as a brown solid. MS (ESI−:336.3[M−H]−).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07528158B2
Source datasetuspto-grants-2009_05
ORD IDord-c20c62834ee04242b1eb7e9c6d2da3d7
Source noteuspto-grants-2009_05