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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2229173Generated: October 31, 2026

Sodium hydride → ethyl (E)-3-[1-(1-methylethyl)-1,2,3,4-tetrahydroquinolin-6-yl]-2-fluoro-2-butenoate

https://huagongshe.com/reaction/2229173

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium hydrideHCID 24758—
ReactantAmmonium ChlorideHCID 25517—
ReactantTriethyl 2-fluoro-2-phosphonoacetateHCID 2734865—
Reactant1-[1-(1-Methylethyl)-1,2,3,4-tetrahydroquinolin-6-yl)ethanoneHCID 10775150—
SolventDimethylformamideHCID 6228—
Productethyl (E)-3-[1-(1-methylethyl)-1,2,3,4-tetrahydroquinolin-6-yl]-2-fluoro-2-butenoateHCID 10852120—

Reaction Steps

450 mg (60%, 12 mmol) of sodium hydride was suspended in 10 ml of N,N-dimethylformamide. 3.3.g (14 mmol) of ethyl 2-fluoro-diethylphosphonoacetate was dropped into the suspension under cooling with ice. The obtained mixture was stirred under cooling with ice for 30 minutes, followed by the addition of 2.0 g (9.2 mmol) of 1-[1-(1-methylethyl)-1,2,3,4-tetrahydroquinolin-6-yl)ethanone. The obtained mixture was stirred under cooling with ice for one hour, followed by the addition of an aqueous solution of ammonium chloride. The obtained mixture was extracted with ethyl acetate, and the organic phase was washed with a saturated aqueous solution of common salt, dried over anhydrous magnesium sulfate and concentrated in a vacuum. The residue was purified by silica gel column chromatography to give 2.3 g of the title compound as a colorless oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06420363B1
Source datasetuspto-grants-2002_07
ORD IDord-bb196681e37144ebbe43c2d14973748a
Source noteuspto-grants-2002_07