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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

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantSodium CarbonateHCID 10340—
Reactantp-Toluenesulfonic acid monohydrateHCID 521998—
ReactantHCID 58921891HCID 58921891—
SolventAcetoneHCID 180—
Product2-methyl-3-oxo-N-phenethyl-butyramideHCID 1198434652%

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07491728B2
Source datasetuspto-grants-2009_02
ORD IDord-6ef57c5c0c9446d1998d0127978d4ee3
Source noteuspto-grants-2009_02