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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 28741Erstellt: 24. Oktober 2026

Oxalyl chloride → 1-Indanone, 4-bromo-

https://huagongshe.com/de/reaction/28741

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
PatentnummerUS07419994B2
Quelldatensatzuspto-grants-2008_09
ORD IDord-543de17566d64a0daa1a055afa83368e
Quellennotizuspto-grants-2008_09