HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1725567Generated: October 31, 2026
Water → 2-methyl-3-oxo-N-phenethyl-butyramide
https://huagongshe.com/reaction/1725567
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Water | HCID 962 | — |
| Reactant | Sodium Carbonate | HCID 10340 | — |
| Reactant | p-Toluenesulfonic acid monohydrate | HCID 521998 | — |
| Reactant | HCID 58921891 | HCID 58921891 | — |
| Solvent | Acetone | HCID 180 | — |
| Product | 2-methyl-3-oxo-N-phenethyl-butyramide | HCID 11984346 | 52% |
Reaction Steps
2-(2-Methyl-[1,3]dioxolan-2-yl)-N-phenethyl-propionamide of Example 1c (0.40 g, 1.5 mmol) was added to p-toluenesulfonic acid monohydrate (0.48 g, 2.5 mmol) in water (20 mmol) under a nitrogen atmosphere at room temperature. Acetone (20 mL) was added, and the reaction mixture was stirred overnight at room temperature and then heated at 95° C. for 3 h. After cooling to room temperature, the solution was made basic with sodium carbonate (0.5 g). The acetone was removed at room temperature under vacuum and the remaining aqueous material was extracted with dichloromethane (50 mL). The organic layer was washed with water (50 mL), brine (50 mL) and then dried with sodium sulfate. After concentration, the product was purified by crystallization from hexanes-ethyl acetate (1:1) to give 2-methyl-3-oxo-N-phenethyl-butyramide (0.17 g, 52%) as a white solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07491728B2 |
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| Source dataset | uspto-grants-2009_02 |
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| ORD ID | ord-6ef57c5c0c9446d1998d0127978d4ee3 |
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| Source note | uspto-grants-2009_02 |
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