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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 7856Generated: October 25, 2026

2-Butyl-4-chloro-5-methoxy-2-(3-oxopentyl)-1-indanone → 9a-butyl-8-chloro-7-methoxy-4-methyl-1,2,9,9a-tetrahydro-3H-fluoren-3-one

https://huagongshe.com/reaction/7856

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-Butyl-4-chloro-5-methoxy-2-(3-oxopentyl)-1-indanoneHCID 21990911—
SolventAcetic AcidHCID 176—
SolventHydrochloric AcidHCID 313—
SolventEthyl AcetateHCID 8857—
Product9a-butyl-8-chloro-7-methoxy-4-methyl-1,2,9,9a-tetrahydro-3H-fluoren-3-oneHCID 2199087660.6%

Reaction Conditions

Temperature90 °C

Reaction Steps

A solution of 2-butyl-4-chloro-5-methoxy-2-(3-oxo-pentyl)-1-indanone (250 mg, 0.74 mmol) in acetic acid (2 mL) was diluted with 6N aqueous HCl (2 mL). The resulting mixture was stirred and heated in an oil bath at 90° C. for 18 hours, then kept at room temperature for 2 days. The mixture was diluted with EtOAc (20 mL), washed with water (30 mL), 5% NaHCO3 (10 mL) and brine (5 mL), dried over MgSO4, filtered, and evaporated under vacuum to an oil (250 mg). The crude product was purified by preparative layer chromatography on three 0.1×20×20 silica gel GF plates, developing with 5% EtOAc in CH2Cl2, to afford 9a-butyl-8-chloro-7-methoxy-4-methyl-1,2,9,9a-tetrahydro-3H-fluoren-3-one (143 mg).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07087599B2
Source datasetuspto-grants-2006_08
ORD IDord-6121252028114c99b582eb81c90945f8
Source noteuspto-grants-2006_08