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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1693184Generated: November 2, 2026

Water → HCID 57827762, compound

https://huagongshe.com/reaction/1693184

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantAmmonium ChlorideHCID 25517—
Reactant1-Bromo-2-fluorobenzeneHCID 61259—
ReactantTetrahydrofuran tolueneHCID 22635083—
ReactantButyllithiumHCID 178418339—
SolventTolueneHCID 1140—
SolventHexaneHCID 8058—
SolventEthyl AcetateHCID 8857—
ProductHCID 57827762HCID 57827762—

Reaction Steps

A solution of n-butyllithium in hexane (2.60 M; 6.05 mL) was added dropwise to a solution containing 2-bromofluorobenzene (1.79 mL) in tetrahydrofuran/toluene (2.88 mL/28.8 mL) under a nitrogen atmosphere at −78° C. The reaction solution was stirred at the same temperature for 10 minutes. A boron trifluoride-diethyl ether complex (1.94 mL) and a solution containing the compound obtained in Preparation Example 22-(2) (1.00 g) in toluene (10 mL) were added dropwise to the reaction solution sequentially at the same temperature. After stirring at the same temperature for one hour, aqueous ammonium chloride was added to the reaction solution, and the reaction solution was warmed to room temperature. Water and ethyl acetate were added to the reaction solution, and the organic layer was separated. The organic layer was washed with a saturated sodium chloride solution. The organic layer was dried over anhydrous magnesium sulfate, and the insoluble matter was separated by filtration. The filtrate was concentrated and the residue was purified by silica gel column chromatography to obtain the title compound (1.60 g).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08158620B2
Source datasetuspto-grants-2012_04
ORD IDord-74b95178a1464fa6ac74a65bdfcb31aa
Source noteuspto-grants-2012_04