HuagongsheHuagongshe Chemistry Print Report · For research reference only
Ethyl ketone → HCID 59443018, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Ethyl ketone | HCID 7288 | — |
| Reactant | Sodium Bicarbonate | HCID 516892 | — |
| Reactant | p-Toluenesulfonic acid monohydrate | HCID 521998 | — |
| Reactant | 2-Hydroxy-4-nitrobenzamide | HCID 68485561 | — |
| Solvent | Toluene | HCID 1140 | — |
| Product | HCID 59443018 | HCID 59443018 | — |
Reaction Steps
A suspension of the compound obtained in (1) described above (5 g), 3-pentanone (6.6 g) and p-toluenesulfonic acid monohydrate (1.6 g) in toluene (70 mL) was heated under reflux overnight. The reaction mixture was poured into a saturated aqueous solution of sodium bicarbonate (100 mL) and the mixture was extracted with ethyl acetate (100 mL×3). The combined organic layer was washed with brine, dried over sodium sulfate and concentrated in vacuo. The resultant residue was recrystallized from ethyl acetate/dichloromethane (1:1) to give the titled compound (5 g) as a colorless powder.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08258131B2 |
| Source dataset | uspto-grants-2012_09 |
| ORD ID | ord-9bfe7d5bd27e45beba467467a03dbdea |
| Source note | uspto-grants-2012_09 |