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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1191682Generated: October 30, 2026

Sodium hydride → Methyl 2-fluoro-3-(2-furan-3-yl-5-methoxyindol-1-ylmethyl)benzoate

https://huagongshe.com/reaction/1191682

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium hydrideHCID 24758—
ReactantAmmonium ChlorideHCID 25517—
ReactantMethyl 3-(bromomethyl)-2-fluorobenzoateHCID 22050044—
Reactant2-Furan-3-yl-5-methoxyindoleHCID 69671146—
SolventDimethylformamideHCID 6228—
SolventMethylenechloride HexaneHCID 21226440—
ProductMethyl 2-fluoro-3-(2-furan-3-yl-5-methoxyindol-1-ylmethyl)benzoateHCID 6967088520.2%

Reaction Steps

To a solution of 2-furan-3-yl-5-methoxyindole (200 mg) in N,N-dimethylformamide (4.7 mL) was added sodium hydride (dispersed in liquid paraffin, minimum 55%, 62 mg) under cooling with ice, and the mixture was stirred at room temperature for one hour. Then a solution of methyl 3-bromomethyl-2-fluorobenzoate (278 mg) in N,N-dimethylformamide (0.2 mL) was added, and the mixture was stirred at 80° C. for 15 hours. The reaction mixture was allowed to cool to ambient temperature. A saturated aqueous ammonium chloride solution-water (2/1) were added to the reaction mixture and this resulting mixture was extracted with ethyl acetate. The organic layer was washed successively with water and saturated saline, dried over anhydrous sodium sulfate and concentrated under reduced pressure. The residue was purified by aminopropylated silica gel column chromatography (eluting solvent: ethyl acetate-hexane) to obtain the title compound (72 mg).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08680120B2
Source datasetuspto-grants-2014_03
ORD IDord-5b1b55b0c7df4cb9bbdc8ca0600bb995
Source noteuspto-grants-2014_03