Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Sulfuric Acid | HCID 1118 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | 4-(4-Acetamidophenyl)-4-oxobutanoic acid | HCID 232337 | — |
| Reactant | Sodium Acetate | HCID 517045 | — |
| Reactant | HCID 20330966 | HCID 20330966 | — |
| Solvent | Methanol | HCID 887 | — |
| Solvent | Water | HCID 962 | — |
| Product | HCID 20331137 | HCID 20331137 | — |
Reaction Steps
A mixture of 35 g. of 3-(4-acetamidobenzoyl)propionic acid, 700 ml. of methanol and 1.4 ml. of concentrated sulfuric acid is refluxed for 76 hours. The solution is cooled to 35° C. and poured onto 7 g. of anhydrous sodium acetate while stirring. The reaction mixture is stirred in an ice-bath. The solid is collected and washed with cold methanol to yield methyl 3-(4-aminobenzoyl)priopionate as a white solid. A mixture of this solid, 9.2 g. of 13-(4-chlorophenyl)tridec-12-ynyl bromide and 4.2 g. of potassium carbonate is stirred for 20 hours at 125° C. under nitrogen. The mixture is then cooled to 25° C. and 30 ml. of water is added. After stirring, the product is filtered and washed with water. Recrystallization from methanol affords methyl 3-{4-[13-(4-chlorophenyl)tridec-12-ynylamino]benzoyl}propionate as a white solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04211783 |
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| Source dataset | uspto-grants-1980_07 |
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| ORD ID | ord-e6c99ce5844e4d078178f04cc7629bd0 |
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| Source note | uspto-grants-1980_07 |
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