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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 18996Erstellt: 25. Oktober 2026

Water → (E)-4-bromo-3-(2-chloro-phenoxy)-but-2-enoic acid ethyl ester

https://huagongshe.com/reaction/18996

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktWaterHCID 962—
EduktN-bromobutanimideHCID 67184—
Edukt(E)-3-(2-chloro-phenoxy)-but-2-enoic acid ethyl esterHCID 66894719—
Katalysator2,2'-Azobis(2,4-dimethylvaleronitrile)HCID 91537—
LösungsmittelDichloromethaneHCID 6344—
Produkt(E)-4-bromo-3-(2-chloro-phenoxy)-but-2-enoic acid ethyl esterHCID 66895331113%

Reaktionsschritte

To a solution of (E)-3-(2-chloro-phenoxy)-but-2-enoic acid ethyl ester (1880 g, 7.82 mol) in dichloromethane (18.6 L) was added N-bromosuccinimide (1490 g, 8.29 mol) and 2,2′-azobis(2,4-dimethylvaleronitrile) (47 g, 0.188 mol) and the resulting solution heated to reflux for 23 h. The light yellow solution was cooled to room temperature and transferred to an extractor before water (19 L) was added. The biphasic mixture was stirred at room temperature for 1 h. The mixture was separated and the organic phase washed with a 20% sodium chloride solution (19 L). The solution was evaporated to give (E)-4-bromo-3-(2-chloro-phenoxy)-but-2-enoic acid ethyl ester (87.8% pure by HPLC, 2824 g, 99%) as a red oil.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS07741327B2
Quelldatensatzuspto-grants-2010_06
ORD IDord-1cf7c89fa3a8465e90568a968c046442
Quellennotizuspto-grants-2010_06