Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Isopropylamine | HCID 6363 | — |
| Reactant | Oxalyl chloride | HCID 65578 | — |
| Reactant | HCID 68984650 | HCID 68984650 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | HCID 68989846 | HCID 68989846 | — |
Reaction Steps
In 2.5 ml of methylene chloride is dissolved 0.25 g of 3-isobutoxy-4-[4-isobutoxy-3-(3-methoxy-3-oxopropyl)benzoyl]benzoic acid. At ambient temperature, 60 μl of oxalyl chloride is added and then 20 μl of N,N-dimethylformamide is added, and the mixture thus obtained is stirred at ambient temperature for one hour. The reaction mixture is cooled with ice water, 0.12 ml of isopropylamine is dropwise added thereto, and the mixture thus obtained is stirred at ambient temperature for one hour. Ethyl acetate and water are added to the reaction mixture, pH is adjusted to 2 with 2 mol/L hydrochloric acid, and the organic layer is separated. The organic layer is washed with water and saturated aqueous solution of sodium chloride successively and dried over anhydrous magnesium sulfate, and the solvent is distilled off under reduced pressure to obtain 0.12 g of methyl 3-(2-isobutoxy-5-{2-isobutoxy-4-[(isopropylamino)carbonyl]benzoyl}-phenyl)propanoate as a white solid product.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07314888B1 |
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| Source dataset | uspto-grants-2008_01 |
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| ORD ID | ord-4f21933e632f4e7b8335ce48131681f9 |
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| Source note | uspto-grants-2008_01 |
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