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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 984725Generated: October 30, 2026

4-Bromoanisole → HCID 69808862, compound

https://huagongshe.com/reaction/984725

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-BromoanisoleHCID 7730—
ReactantBinap, (A+-)-HCID 634876—
ReactantSodium n-butylateHCID 23669364—
Reactant2-methyl-5-(N-methyl-anilinomethylene) cyclopentanoneHCID 53960153—
CatalystBis(dibenzylideneacetone)palladiumHCID 9811564—
SolventTolueneHCID 1140—
ProductHCID 69808862HCID 6980886255%

Reaction Steps

An oven dried Schlenk tube equipped with a rubber septum was cooled under an argon purge. The septum was removed and the tube was charged with tris(dibenzylideneacetone)dipalladium (0) (11.5 mg, 0.025 mmol, 5 mol % Pd), (S)-BINAP (31.4 mg, 0.05 mmol, 10 mol %) and 2-methyl-5-(N-methyl-anilinomethylene)cyclopentanone (108 mg, 0.5 mmol). Toluene (2 mL) was added and the mixture was stirred for 1 min at room temperature. 4-Bromoanisole (187 mg, 1.0 mmol) and sodium 1-butoxide (96 mg, 1.0 mmol) were added to the tube. The tube was capped with the septum, purged with argon, and additional toluene (4 mL) was added through the septum. The mixture was heated to 100° C. with stirring until the starting ketone had been completely consumed as judged by GC analysis. The mixture was cooled to room temperature, quenched with saturated aqueous ammonium chloride (10 mL) and diluted with ether (20 mL). The mixture was poured into a separatory funnel and the layers were separated. The aqueous layer was extracted with ether (20 mL), and the combined organic layers were washed with brine (20 mL), dried over anhydrous magnesium sulfate, filtered, and concentrated in vacuo. The crude material was purified by flash chromatography on silica gel to afford 88 mg (55%) of the title compound. The ee was determined to be 62% by chiral HPLC analysis.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06867310B1
Source datasetuspto-grants-2005_03
ORD IDord-71345e8e84324b3c82baee2f548b181b
Source noteuspto-grants-2005_03