HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1518745Generated: October 27, 2026
p-Bromochlorobenzene → Ethyl 5-(4-chlorophenyl)-3-(4-sulfamoylphenyl)furan-2-carboxylate
https://huagongshe.com/reaction/1518745
Participants
| Role | Name | HCID | Charge |
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| Reactant | p-Bromochlorobenzene | HCID 7806 | — |
| Reactant | Potassium Acetate | HCID 517044 | — |
| Reactant | Ethyl 3-(4-sulfamoylphenyl)furan-2-carboxylate | HCID 68285772 | — |
| Catalyst | palladium(II) acetate | HCID 167845 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Solvent | Dimethylacetamide | HCID 31374 | — |
| Product | Ethyl 5-(4-chlorophenyl)-3-(4-sulfamoylphenyl)furan-2-carboxylate | HCID 60169459 | 9.8% |
Reaction Steps
1-bromo-4-chlorobenzene (0.214 g, 1.11 mmol) and potassium acetate (0.199 g, 2.03 mmol) were added to a solution of ethyl 3-(4-sulfamoylphenyl)furan-2-carboxylate (60a, 0.3 g, 1.01 mmol) in dimethyl acetamide (5 ml) at 25° C. in a tube. A nitrogen gas was bubbled through the reaction mixture for 15 minutes. To the reaction mixture was then added palladium (II) acetate (0.023 gm, 0.102 mmol) under nitrogen atmosphere and the tube was sealed. The reaction mixture was then heated at 150° C. for 20 hr with stirring. The progress of the reaction was monitored by TLC. The reaction mixture was then cooled to 25° C. and concentrated under reduced pressure. The residue so obtained was dissolved in ethyl acetate (30 ml). The solution so obtained was then washed with water (2×10 ml), dried over sodium sulphate and concentrated under reduced pressure to obtain a crude product, which was then purified by flash column chromatography using 50% ethyl acetate in hexanes as an eluent to obtain the title compound (0.040 gm, 9.70%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09072731B2 |
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| Source dataset | uspto-grants-2015_07 |
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| ORD ID | ord-533e343b90364337b2fa4b0dcb197104 |
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| Source note | uspto-grants-2015_07 |
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