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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 9281Erstellt: 24. Oktober 2026

Oxalyl chloride → 1-Indanone, 4-bromo-

https://huagongshe.com/de/reaction/9281

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktOxalyl chlorideHCID 65578—
Edukt3-(2-Bromophenyl)propionic acidHCID 316010—
EduktAluminum(III) ChlorideHCID 6451240—
KatalysatorDimethylformamideHCID 6228—
LösungsmittelDichloromethaneHCID 6344—
Produkt1-Indanone, 4-bromo-HCID 98713—

Reaktionsbedingungen

Temperatur0 °C

Reaktionsschritte

4-Bromo-indan-1-one was obtained by the following procedure: A solution of 3-(2-bromo-phenyl)-propionic acid (commercially available from Oakwood Products) (15.0 g, 65.5 mmol) in CH2Cl2 at 0° C. was reacted with oxalyl chloride (7.2 mL, 1.5 eq) followed by 2–3 drops of DMF. The mixture was stirred until no more gas evolution was observed. As the mixture was concentrated and the residue was dissolved in CH2Cl2, cooled to 0° C., and treated with AlCl3 (9.6 g, 1.1 eq). After 1 h the mixture was quenched with water and the layers were separated. The aqueous layer was extracted with Et2O (3×150 mL) and the combined organic extracts were washed with H2O (3×100 mL), saturated NaHCO3 (3×100 mL), brine (1×100 mL), dried over MgSO4 and concentrated. 4-Bromoindan-1-one, 10.5 g (76%) was obtained by chromatography using 10% EtOAc:hexane as eluant. Use of 4-bromo-indan-1-one in Method NINETEEN produced 4-(4-bromo-indan-2-yl)-1,3-dihydro-imidazole-2-thione (Compound 149).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS07091232B2
Quelldatensatzuspto-grants-2006_08
ORD IDord-39187aa04b4741c7af65c404933627df
Quellennotizuspto-grants-2006_08