Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Sulfuric Acid | HCID 1118 | — |
| Reactant | Acetic Anhydride | HCID 7918 | — |
| Reactant | HCID 11108632 | HCID 11108632 | — |
| Solvent | Water | HCID 962 | — |
| Product | HCID 10999783 | HCID 10999783 | 34.8% |
Reaction Steps
In a 100 mL flask, 4-oxo-3-(3-phenyl-propionylamino)-pentanoic acid methyl ester (10 g, 36 mmol) and acetic anhydride (28 mL) were combined. Following addition of concentrated H2SO4 (1 mL), the solution was heated to 90° C. for 30 min and cooled to ambient temperature. The reaction was slowly diluted with DI water (30 mL, potential exotherm). The reaction mixture was partitioned between CH2Cl2 (150 mL) and water (150 mL). The organic phase was washed with DI water, 10% NaHCO3 (aq), brine (150 mL), and then was dried (MgSO4) and concentrated to a brown oil. The residue was purified by column chromatography (600 mL SiO2, 35% EtOAc/hexanes) to provide the desired product (3.25 g) as a pale yellow oil. 1H NMR (400 MHz, CDCl3) δ 7.33-7.20 (m, 5H), 3.72 (s, 3H), 3.47 (s, 2H), 3.08-2.96 (m, 4H), 2.24 (s, 3H); MS (EI+) 260 (M+H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07282501B2 |
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| Source dataset | uspto-grants-2007_10 |
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| ORD ID | ord-3413087edbb4491a8e88a1db9826a0a6 |
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| Source note | uspto-grants-2007_10 |
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