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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1920807Generated: October 29, 2026

Hydrochloric Acid → HCID 58572760, compound

https://huagongshe.com/reaction/1920807

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantStannane, tributyl(1-ethoxyethenyl)-HCID 619414—
Reactant2-Bromo-4-fluoro-6-methoxybenzenamineHCID 58572744—
Solvent1,4-DioxaneHCID 31275—
ProductHCID 58572760HCID 5857276070%

Reaction Conditions

Temperature100 °C

Reaction Steps

To a solution of 2-bromo-4-fluoro-6-methoxy aniline (4.80 g, 21.8 mmol), which had been obtained in Reference example 5 (5a), in 1,4-dioxane (200 mL), tributyl (1-ethoxy vinyl) tin (11.1 mL, 32.7 mmol) and tetrakistriphenyl phosphine palladium (2.52 g, 2.18 mmol) were added, and the mixture was stirred for 16 hours at 100° C. After cooling the reaction solution to room temperature, 1 N aqueous hydrogen chloride solution (100 mL) was added and stirred further for 2 hours. The reaction solution was concentrated under reduced pressure, neutralized by adding 1 N aqueous sodium hydroxide solution, and then extracted with ethyl acetate. The organic layer was washed with saturated brine and dried over anhydrous magnesium sulfate. The solvent was distilled off under reduced pressure. The residue was purified by silica gel chromatography (n-hexane/ethyl acetate=4/1) to give the title compound as a yellow solid substance (2.80 g, yield 70%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08173631B2
Source datasetuspto-grants-2012_05
ORD IDord-b5236c50f6bf4232a15a7a410cb611d4
Source noteuspto-grants-2012_05