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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 30358Erstellt: 23. Oktober 2026

1-Chloro-4-(chloromethyl)benzene → 3-(3-Bromophenyl)-4-(4-chlorophenyl)-3-methyl-2-butanone

https://huagongshe.com/de/reaction/30358

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
Edukt1-Chloro-4-(chloromethyl)benzeneHCID 7723—
EduktEthyl AcetateHCID 8857—
EduktCaesium hydroxide--water (1/1/1)HCID 23679066—
Edukt3-(3-Bromophenyl)butan-2-oneHCID 66436791—
KatalysatorTetrabutylammonium IodideHCID 67553—
LösungsmittelWaterHCID 962—
LösungsmittelDichloromethaneHCID 6344—
Produkt3-(3-Bromophenyl)-4-(4-chlorophenyl)-3-methyl-2-butanoneHCID 68675648—

Reaktionsschritte

To a solution of 3-(3-bromophenyl)-2-butanone (2.0 g, 8.8 mmol) in methylene chloride (100 mL) was added 4-chlorobenzyl chloride (1.4 g, 8.8 mmol), tetrabutylammonium iodide (0.16 g, 0.44 mmol) and cesium hydroxide monohydrate (5.9 g, 35 mmol). After stirring at room temperature for 3.5 h, the reaction mixture was poured into ethyl acetate (100 mL) and water (100 mL). The organic layer was separated and the aqueous layer extracted with ethyl acetate. The combined organic extracts were washed with brine, dried over magnesium sulfate, filtered, and concentrated to dryness to give the title compound. 1H NMR (400 MHz, CD3OD): δ 7.5-7.1 (m, 4 H), 7.08 (d, 2H), 6.68 (d, 2H), 3.16 (ABq, 2H), 1.98 (s, 3H), 1.42 (s, 3H).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS07423067B2
Quelldatensatzuspto-grants-2008_09
ORD IDord-b7583f5efae64ba4bc4392e03243ee37
Quellennotizuspto-grants-2008_09