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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 7891Generated: October 26, 2026

Tetramethyltin → 2-Butyl-6-fluoro-5-methoxy-4-methyl-1-indanone

https://huagongshe.com/reaction/7891

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTetramethyltinHCID 11661—
ReactantTriphenylphosphineHCID 11776—
ReactantLithium ChlorideHCID 433294—
Reactant4-Bromo-2-butyl-6-fluoro-5-methoxy-1-indanoneHCID 21990906—
CatalystHCID 178418476HCID 178418476—
SolventDimethylformamideHCID 6228—
Product2-Butyl-6-fluoro-5-methoxy-4-methyl-1-indanoneHCID 2199086324.5%

Reaction Conditions

Temperature100 °C

Reaction Steps

A mixture of 4-bromo-2-butyl-6-fluoro-5-methoxy-1-indanone (1.86 g, 5.94 mmol), bis(triphenylphosphine)palladium(II) chloride (208 mg, 0.297 mmol), tetramethyltin (0.989 mL, 7.128 mmol), triphenylphosphine (156 mg, 0.594 mmol), lithium chloride (504 mg, 11.88 mmol), and anhydrous N,N-dimethyl-formamide (11.9 mL) was placed under a nitrogen atmosphere, stirred, and heated in an oil bath at 100° C. for 22 hours. After cooling to room temperature, the mixture was evaporated under vacuum. The residue in EtOAc (150 mL) was washed with water (4×100 mL) and brine (50 mL), dried over MgSO4, filtered, and evaporated under vacuum to an oil (2.15 g). The crude product was purified by chromatography on EM silica gel 60 (2.5×29 cm column), eluting with CH2Cl2 (50 mL fore-run followed by 8 mL fractions). Fractions 20-28 were combined and evaporated under vacuum to provide 2-butyl-6-fluoro-5-methoxy-4-methyl-1-indanone (365 mg) as an oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07087599B2
Source datasetuspto-grants-2006_08
ORD IDord-270913168eb241f99a23be25455ccdcc
Source noteuspto-grants-2006_08