HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1844089Generated: November 1, 2026
1-Chloro-4-iodobenzene → HCID 67975703, compound
https://huagongshe.com/reaction/1844089
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 1-Chloro-4-iodobenzene | HCID 12510 | — |
| Reactant | Potassium Phosphate, Tribasic | HCID 62657 | — |
| Reactant | HCID 67975699 | HCID 67975699 | — |
| Catalyst | Tetrabutylammonium Bromide | HCID 74236 | — |
| Catalyst | HCID 178419072 | HCID 178419072 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 67975703 | HCID 67975703 | — |
Reaction Steps
To a solution of tetrahydro-1H-indeno[1,2-b]pyrrol-2-one (1.00 g, 5.77 mmol) in water (3 mL) was added copper (I) oxide (167 mg), p-chloroiodobenzene (1.38 g, 5.77 mmol), tetrabutylammonium bromide (0.372 g, 1.15 mmol) and potassium phosphate (2.45 g, 11.5 mmol). The suspension was vigorously stirred at 130° C. overnight. The mixture was cooled down and diluted with dichloromethane. The solid were filtered off and the organic layer was dried and concentrated. The residue was purified by flash chromatography with a gradient of ethyl acetate in cyclohexane of 1 to 60%, to give the desired product F16 (600 mg, 39%). LCMS (method A) 1.72 min; ES+: 284 (M+H+).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08946280B2 |
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| Source dataset | uspto-grants-2015_02 |
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| ORD ID | ord-d587816812ba420cb378ede02f8a045d |
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| Source note | uspto-grants-2015_02 |
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