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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 7890Generated: October 26, 2026

Methyl iodide → 4-Bromo-2-butyl-6-fluoro-5-methoxy-1-indanone

https://huagongshe.com/reaction/7890

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethyl iodideHCID 6328—
ReactantSodium BicarbonateHCID 516892—
Reactant4-Bromo-2-butyl-6-fluoro-5-hydroxy-1-indanoneHCID 21990852—
SolventDimethylformamideHCID 6228—
Product4-Bromo-2-butyl-6-fluoro-5-methoxy-1-indanoneHCID 2199090681.6%

Reaction Steps

A mixture of 4-bromo-2-butyl-6-fluoro-5-hydroxy-1-indanone (2.17 g, 7.23 mmol), N,N-dimethylformamide (14.5 mL), methyl iodide (0.675 mL, 10.84 mmol), and sodium bicarbonate (1.50 g, 18.1 mmol) was stirred at room temperature for 17 hours. The solvent was evaporated under vacuum. The residue in EtOAc (150 mL) was washed with water (5×100 mL) and brine (50 mL), dried over MgSO4, filtered, and evaporated under vacuum to an oil (2.29 g). The crude product was dissolved in CH2CL2 (5 mL) and the solution filtered through a pad of EM silica gel 60 (20 mL) using an additional 60 mL of CH2Cl2 to elute the silica gel. The CH2Cl2 filtrate was evaporated under vacuum to afford 4-bromo-2-butyl-6-fluoro-5-methoxy-1-indanone (1.86 g) as a pink oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07087599B2
Source datasetuspto-grants-2006_08
ORD IDord-835f01ea929a484fbdde0611e5ce74b3
Source noteuspto-grants-2006_08