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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1874050Generated: October 31, 2026

2-Methyl-2-butene → HCID 58492412, compound

https://huagongshe.com/reaction/1874050

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-Methyl-2-buteneHCID 10553—
ReactantSodium ChloriteHCID 23668197—
Reactant3-[5-Fluoro-3-(4-methoxyphenyl)-4-oxo-8-propoxy-4H-quinolin-1-yl]propionaldehydeHCID 58492425—
ReactantCID 86658926HCID 86658926—
SolventWaterHCID 962—
SolventDichloromethaneHCID 6344—
Solventtert-ButanolHCID 6386—
ProductHCID 58492412HCID 5849241268.1%

Reaction Steps

3-[5-Fluoro-3-(4-methoxyphenyl)-4-oxo-8-propoxy-4H-quinolin-1-yl]propionaldehyde (1.0 g, 2.61 mmol) was dissolved in water (10 ml), tert-butyl alcohol (20 ml) and dichloromethane (20 ml). Sodium chlorite (3.2 g, 35.4 mmol), 2-methyl-2-butene (19.86 gm, 283 mmol) and sodium-dihydrogenphosphate dihydrate (2 g, 2.61 mmol) were added to the resulting solution, and the solution was stirred at room temperature for 1 hour. Water was added to the reaction mixture, the mixture was extracted with dichloromethane, and then washed with water and dried over anhydrous sodium sulfate. The dried product was concentrated under reduced pressure. The residue was purified using silica gel column chromatography (dichloromethane:ethyl acetate=50:50→0:100). The purified product was concentrated to dryness under reduced pressure, giving a pale yellow powder of 3-[5-fluoro-3-(4-methoxyphenyl)-4-oxo-8-propoxy-4H-quinolin-1-yl]propionic acid (710 mg, yield: 68%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08304546B2
Source datasetuspto-grants-2012_11
ORD IDord-3e66ed18a727432291f1c0b76e405331
Source noteuspto-grants-2012_11