HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1372512Generated: November 1, 2026
1-Penten-3-one → 5-Amino-2-butyl-6-fluoro-2-(3-oxopentyl)-1-indanone
https://huagongshe.com/reaction/1372512
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 1-Penten-3-one | HCID 15394 | — |
| Reactant | Sodium Methoxide | HCID 10942334 | — |
| Reactant | 5-Amino-2-butyl-6-fluoro-1-indanone | HCID 17972717 | — |
| Solvent | Ethanol | HCID 702 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | 5-Amino-2-butyl-6-fluoro-2-(3-oxopentyl)-1-indanone | HCID 21072006 | 217.4% |
Reaction Steps
A solution of 5-amino-2-butyl-6-fluoro-1-indanone (0.81 g, 3.84 mmol) in ethanol (18 mL) was treated with sodium methoxide (0.5M solution in MeOH, 1.54 mL, 0.768 mmol) and ethyl vinyl ketone (0.572 mL, 5.76 mmol). The resulting solution was stirred under a nitrogen atmosphere and heated in an oil bath at 70° C. over night. After cooling to room temperature, the mixture was diluted with CH2Cl2 and filtered through a pad of silica gel. The product washed off with EtOAc and the filtrate was evaporated under vacuum. The residue was purified by flash chromatography on a Biotage 40M KP-Sil column, eluting with 4:1 to 3:1 hexanes-EtOAc. The product containing fractions were evaporated under vacuum to provide to afford 5-amino-2-butyl-6-fluoro-2-(3-oxopentyl)-1-indanone(0.51 g, 45%) as a yellow foam.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US07157604B2 |
|---|
| Source dataset | uspto-grants-2007_01 |
|---|
| ORD ID | ord-051c2020debf4a59a6bc8f99ce07ccd5 |
|---|
| Source note | uspto-grants-2007_01 |
|---|