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
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | alpha-Bromo-o-chlorotoluene | HCID 11905 | — |
| Reactant | HCID 86604125 | HCID 86604125 | — |
| Solvent | Water | HCID 962 | — |
| Product | 6-Chloro-1-(2-chloro-benzyl)-5-nitro-1,2-dihydro-indazol-3-one | HCID 68831736 | — |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07528158B2 |
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| Source dataset | uspto-grants-2009_05 |
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| ORD ID | ord-c20c62834ee04242b1eb7e9c6d2da3d7 |
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| Source note | uspto-grants-2009_05 |
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