HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1454185Generated: November 3, 2026
Hydrochloric Acid → Methyl 3-acetyl-5-(dipropylcarbamoyl)benzoate
https://huagongshe.com/reaction/1454185
Participants
| Role | Name | HCID | Charge |
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| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Butyl vinyl ether | HCID 8108 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | 1,3-Bis(diphenylphosphino)propane | HCID 81219 | — |
| Reactant | Methyl 3-bromo-5-(dipropylcarbamoyl)benzoate | HCID 21939662 | — |
| Catalyst | palladium(II) acetate | HCID 167845 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | Methyl 3-acetyl-5-(dipropylcarbamoyl)benzoate | HCID 57529297 | — |
Reaction Steps
A mixture of methyl 3-bromo-5-(dipropylcarbamoyl)benzoate (342 mg, 1.0 mmol), 1-(vinyloxy)butane (200.4 mg, 0.26 mL, 2.0 mmol), palladium acetate (6.68 mg, 0.030 mmol), DPPP (27.2 mg, 0.066 mmol) and potassium carbonate (166 mg, 1.2 mmol) in DMF (2.5 mL) and H2O (0.3 mL) in a Smith process vial was heated at 122° C. in microwave for 3 h. The reaction mixture was cooled down to RT and hydrolyzed by addition of 5% HCl slowly. The reaction mixture was worked up by extraction with ethyl acetate and concentration under vacuum. The crude mixture was purified by reverse phase prep HPLC to give the title compound: HPLC retention time: 1.805 min (method A). MS (ESI) (M+H)+ 306.26.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07476764B2 |
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| Source dataset | uspto-grants-2009_01 |
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| ORD ID | ord-3c5ca06440cf4d33be52748d1a14560c |
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| Source note | uspto-grants-2009_01 |
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