HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1015622Generated: October 31, 2026
2,4-Dichlorobenzoyl chloride → HCID 67299348, compound
https://huagongshe.com/reaction/1015622
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 2,4-Dichlorobenzoyl chloride | HCID 66645 | — |
| Reactant | HCID 20775770 | HCID 20775770 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Solvent | Sodium Bicarbonate | HCID 516892 | — |
| Product | HCID 67299348 | HCID 67299348 | 78% |
Reaction Steps
To a stirred solution of 5-Phenyl-3-{[5-(3-trifluoromethyl-phenyl)-furan-2-ylmethyl]-amino}-thiophene-2-carboxylic acid methylester (65 mg 0.142 mmol) in dichloromethane (3 ml) and saturated NaHCO3 solution (3 ml) was added a solution of 2,4-dichloro-benzoyl chloride (36 mg, 1.2 eq.) in dichloromethane (0.9 ml). The reaction mixture was stirred vigorously at room temperature for overnight. The organic phase was collected and the aqueous phase was extracted twice with methylene chloride (2×15 ml). The organic layers were combined, washed with water, brine and dried over anhydrous Na2SO4. Solvent was removed and residue was purified on silica gel using Hexane:EtOAc 9:1 as eluant to give the desired product in 78% yield (70 mg). The proton NMR indicated the presence of rotamers.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07985769B2 |
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| Source dataset | uspto-grants-2011_07 |
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| ORD ID | ord-25d3093b2f104848a06c0d0f743997cf |
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| Source note | uspto-grants-2011_07 |
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