HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1673458Generated: October 30, 2026
Sodium Carbonate → Tert-butyl 2-(benzamido)-4-(3-chlorophenyl)benzoate
https://huagongshe.com/reaction/1673458
Participants
| Role | Name | HCID | Charge |
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| Reactant | Sodium Carbonate | HCID 10340 | — |
| Reactant | (3-Chlorophenyl)boronic acid | HCID 2734323 | — |
| Reactant | Tert-butyl 2-(benzamido)-4-bromobenzoate | HCID 67343005 | — |
| Catalyst | dicyclohexylphenylphosphine palladium(II) | HCID 86634613 | — |
| Solvent | Dimethylacetamide | HCID 31374 | — |
| Product | Tert-butyl 2-(benzamido)-4-(3-chlorophenyl)benzoate | HCID 67344272 | — |
Reaction Steps
44 mp of 3-chlorophenylboronic acid, 49 mg of sodium carbonate and 6 mg of polymer supported di(acetato)dicyclohexylphenylphosphine palladium(II) were added to 2.5 mL of N,N-dimethylacetamide solution containing 70 mg of tert-butyl 2-(benzamido)-4-bromobenzoate, and stirred at 90° C. for 15 hours. After the reaction mixture was cooled to room temperature, 5.1 mg of polymer supported di(acetato) dicyclohexylphenylphosphine palladium(II) was added and stirred at 110° C. for 9 hours and 30 minutes. After the reaction mixture was cooled to room temperature, insoluble were removed by filtration and ethyl acetate and 10% citric acid aqueous solution were added. The organic layer was separated and dried over anhydrous magnesium sulfate after washed with 10% citric acid aqueous solution and a saturated sodium chloride aqueous solution sequentially, and the solvent was evaporated under reduced pressure. The obtained residue was purified with silica gel column chromatography [Flash Tube 2008 manufactured by Tribonex Company, eluent; hexane:ethyl acetate=4:1] to obtain tert-butyl 2-(benzamido)-4-(3-chlorophenyl)benzoate.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07999132B2 |
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| Source dataset | uspto-grants-2011_08 |
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| ORD ID | ord-4cbafd099ab44f56adacf567cc1c12ba |
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| Source note | uspto-grants-2011_08 |
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