Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Propionic Acid | HCID 1032 | — |
| Reactant | Methyl Ethyl Ketone | HCID 6569 | — |
| Reactant | m-Toluidine | HCID 7934 | — |
| Reactant | Sodium borohydride | HCID 4311764 | — |
| Product | HCID 21993246 | HCID 21993246 | — |
Reaction Steps
3-Toluidine (107.16 g), 2-butanone (72.11 g) and propionic acid (74.08 g) were stirred and cooled to 0° C. Sodium borohydride (37.83 g) was then added in portions keeping the temperature below 5° C. After allowing to warm to room temperature the reaction mixture was carefully poured onto ice/water. The product was extracted into ethyl acetate, washed with water, 2% hydrochloric acid and finally water again before drying over magnesium sulphate. Evaporation of the solvent under reduced pressure gave a brown oil which was purified by chromatography on silica gel.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06235096B1 |
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| Source dataset | uspto-grants-2001_05 |
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| ORD ID | ord-57533be3b7fc4339b65f080dd2f5ca8c |
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| Source note | uspto-grants-2001_05 |
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