HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 891322Generated: October 30, 2026
Carbon Tetrachloride → HCID 21933937, compound
https://huagongshe.com/reaction/891322
Participants
| Role | Name | HCID | Charge |
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| Reactant | Carbon Tetrachloride | HCID 5943 | — |
| Reactant | N-bromobutanimide | HCID 67184 | — |
| Reactant | HCID 21934174 | HCID 21934174 | — |
| Catalyst | Benzoyl Peroxide | HCID 7187 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | HCID 21933937 | HCID 21933937 | 74% |
Reaction Steps
To a heterogeneous, refluxing solution of 2-(4-fluorophenyl)-4-methyl-5-[4-(methylsulfonyl)phenyl]-3(2H)-pyridazinone (590 mg, 1.65 mmol) and carbon tetrachloride (24 mL) was quickly added N-bromosuccinimide (yield: 308 mg, 1.73 mmol) followed by benzoyl peroxide (12 mg, 0.05 mmol). After 1 hour the reaction had only run to near 50% completion. Additional benzoyl peroxide (12 mg, 0.05 mmol) was added, and the reaction checked after another 1 hour. The reaction was still not complete, and so more benzoyl peroxide (4 mg, 0.017 mmol) was added. After 30 minutes, the reaction was completed. The mixture was cooled to 23° C. and diluted with ethyl acetate. The acetate solution was washed with saturated NaHCO3, water, and brine. The solution was dried over MgSO4, filtered, and concentrated in vacuo. The residue was chromatographed (flash silica gel, ethyl acetate/hexanes gradient 1:1 to 4:1) to provide the product (yield: 530 mg, 74%). 1H NMR (300 MHz, CDCl3) δ 3.16 (s, 3H), 4.34 (s, 2H), 7.20 (dd, J=8.8, 8.8 Hz, 2H), 7.67-7.74 (m, 2H), 7.82 (d, J=8.7 Hz, 2H), 7.86 (s, 1H), 8.17 (d, J=8.7 Hz, 2H). MS (APCI+) m/z 437 (M+H)+.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07001895B2 |
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| Source dataset | uspto-grants-2006_02 |
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| ORD ID | ord-44eedd284d3945cbb73f3e743e0caf3d |
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| Source note | uspto-grants-2006_02 |
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