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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1372511Generated: November 2, 2026

Acetic Acid → 7-amino-9a-butyl-6-fluoro-1,2,9,9a-tetrahydro-3H-fluoren-3-one

https://huagongshe.com/reaction/1372511

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetic AcidHCID 176—
ReactantPyrrolidineHCID 31268—
Reactant5-Amino-2-butyl-6-fluoro-2-(3-oxobutyl)-1-indanoneHCID 17972707—
SolventTolueneHCID 1140—
Product7-amino-9a-butyl-6-fluoro-1,2,9,9a-tetrahydro-3H-fluoren-3-oneHCID 1797268180%

Reaction Conditions

Temperature100 °C

Reaction Steps

The diketone from step 1 (0.6 g, 2.14 mmol) was dissolved in toluene (15 mL) and treated with acetic acid (0.236 mL, 4.12 mmol) and pyrrolidine (0.344 mL, 4.12 mmol). The resulting solution was stirred and heated in an oil bath at 100° C. for 1.5 hours. After cooling to room temperature, the mixture was filtered through a pad of silica gel and the product was washed off with EtOAc. The filtrate and washings were concentrated 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 7-amino-9a-butyl-6-fluoro-1,2,9,9a-tetrahydro-3H-fluoren-3-one (0.45 g, 80%) as a yellow solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07157604B2
Source datasetuspto-grants-2007_01
ORD IDord-d126b477d1e245b790ef94cc03d4ccc6
Source noteuspto-grants-2007_01