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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 66285Erstellt: 24. Oktober 2026

Benzoyl Peroxide → Ethyl 2-bromo-2-(3,4-dichlorophenyl)acetate

https://huagongshe.com/de/reaction/66285

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktBenzoyl PeroxideHCID 7187—
EduktN-bromobutanimideHCID 67184—
EduktEthyl 3,4-dichlorophenylacetateHCID 2737422—
LösungsmittelCarbon TetrachlorideHCID 5943—
ProduktEthyl 2-bromo-2-(3,4-dichlorophenyl)acetateHCID 12717583—

Reaktionsschritte

In a three-necked flask fitted with a Nichrome stirrer and a reflux condenser is placed 7.0 g of ethyl 3,4-dichlorophenylacetate, 5.9 g of N-bromosuccinimide, 0.1 g of benzoyl peroxide and 150 ml of carbon tetrachloride. The reaction mixture is heated at reflux for 18 hours, cooled and filtered. The carbon tetrachloride filtrate is concentrated under reduced pressure to give a deep orange liquid. Vacuum distillation at 115°-120° C. (0.5 mm) gives ethyl α-bromo-3,4-dichlorophenylacetate as a pale yellow liquid.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS04131611
Quelldatensatzuspto-grants-1978_12
ORD IDord-8bb4d254d7f440ec8351d60f1eca7e2b
Quellennotizuspto-grants-1978_12