HuagongsheHuagongshe Chemistry Print Report · For research reference only
2-Oxobutanoic Acid → 2-isovaleramidobut-2-enoic acid
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 2-Oxobutanoic Acid | HCID 58 | — |
| Reactant | Water | HCID 962 | — |
| Reactant | Butanamide, 3-methyl- | HCID 10930 | — |
| Solvent | Toluene | HCID 1140 | — |
| Product | 2-isovaleramidobut-2-enoic acid | HCID 6443864 | — |
Reaction Steps
A solution of 1.07 g (10.5 mmole) of 2-ketobutyric acid and 0.71 g (7.0 mmole) of isovaleramide in 15 ml of toluene was stirred under reflux with collection of H2O in a small Dean-Stark trap. After 5 hrs, the solution was cooled, resulting in fairly heavy crystallization. After standing, the solid was collected on a filter and washed with toluene and then with CH2Cl2. Yield of white crystals=0.47 g, mp 172°-174° (slight prelim. softening). The material was recrystallized from diisopropyl ketone. Tlc (4:1 toluene-AcOH) now showed only a faint trace of the other isomer. Yield of white crystals=0.32 g (25%), mp 175° (slight prelim. softening). NMR indicated essentially exclusively Z-isomer.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04880793 |
| Source dataset | uspto-grants-1989_11 |
| ORD ID | ord-3ff1690b44f94974ac533d1af0a1053a |
| Source note | uspto-grants-1989_11 |