HuagongsheHuagongshe Chemistry Print Report · For research reference only
Potassium Hydroxide → 5-Amino-2-butyl-4,6-difluoro-2-(3-oxohexyl)-1-indanone
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Potassium Hydroxide | HCID 14797 | — |
| Reactant | 1-Hexen-3-one | HCID 15395 | — |
| Reactant | HCID 11421253 | HCID 11421253 | — |
| Reactant | 5-Amino-2-butyl-4,6-difluoro-1-indanone | HCID 21072002 | — |
| Solvent | Toluene | HCID 1140 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | 5-Amino-2-butyl-4,6-difluoro-2-(3-oxohexyl)-1-indanone | HCID 21072003 | — |
Reaction Steps
A solution of 5-amino-2-butyl-4,6-difluoro-1-indanone (0.25 g, 1.05 mmol) in toluene (5.5 mL) was treated with potassium hydroxide (0.1 g, 40% w/w), N-[4-(trifluoromethyl)benzy]cinchoninium bromide (0.112 g, 0.21 mmol), and propyl vinyl ketone (0.154 g, 1.57 mmol). The resulting solution was stirred under a nitrogen atmosphere for 2 hours. After being diluted with CH2Cl2, the mixture was filtered through a pad of silica gel and rinsed with EtOAc. The filtrate was evaporated under vacuum to afford crude 5-amino-2-butyl-4,6-difluoro-2-(3-oxohexyl)-1-indanone.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07157604B2 |
| Source dataset | uspto-grants-2007_01 |
| ORD ID | ord-67dbdc916ac9477daab2b0bf929cf0fa |
| Source note | uspto-grants-2007_01 |