Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Sulfuric Acid | HCID 1118 | — |
| Reactant | 4-(4-Aminophenyl)butanoic acid | HCID 27049 | — |
| Reactant | HCID 14451767 | HCID 14451767 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | HCID 86656427 | HCID 86656427 | 84% |
Reaction Steps
The 4-aminophenylbutyramide used in this example was obtained according to patent literature WO 02/08247 A2 or WO 03/051909 A2. Procedure was as follow: Methanol (100 ml) was charged to 4-(4-Aminophenyl)-butyric acid (from Aldrich) CAS[15118-60-2] (FW=179.22, 1 eq, 15 g, 83.7 mmol). Sulphuric acid FW=98.08 (4 eq, 334.8 mmol, 33 g) was added maintaining the temperature below 20° C. The mixture was then refluxed for one hour and concentrated by distillation at atmospheric pressure until half of methanol will be removed. The reaction mixture was then cooled to 50° C. and t-butyl-methyl ether was added maintaining the temperature above 45° C. The mixture was then gradually cooled to 0-5° C. and held at this temperature for 1 hour. The resultant crystalline product was isolated by filtration and washed by cold mixture of methanol and t-butyl-methyl ether (4:10) and cold ether and then dried under vacuum and then dried under vacuum to give methyl 4-aminophenylbutyrate hydrogensulfate as a white crystal (20.0 g, 84%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08487130B2 |
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| Source dataset | uspto-grants-2013_07 |
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| ORD ID | ord-87ab5f99bed74880ad8cc41afd30cf7b |
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| Source note | uspto-grants-2013_07 |
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