Back
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

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1-Penten-3-oneHCID 15394—
ReactantSodium MethoxideHCID 10942334—
Reactant5-Amino-2-butyl-6-fluoro-1-indanoneHCID 17972717—
SolventEthanolHCID 702—
SolventDichloromethaneHCID 6344—
Product5-Amino-2-butyl-6-fluoro-2-(3-oxopentyl)-1-indanoneHCID 21072006217.4%

Reaction Conditions

Temperature70 °C

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07157604B2
Source datasetuspto-grants-2007_01
ORD IDord-051c2020debf4a59a6bc8f99ce07ccd5
Source noteuspto-grants-2007_01