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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1636563Erstellt: 26. Oktober 2026

Chloroacetyl chloride → 2-(4'-Chloroacetamido-3-iodophenyl) benzothiazole

https://huagongshe.com/reaction/1636563

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktChloroacetyl chlorideHCID 6577—
EduktBenzenamine, 4-(2-benzothiazolyl)-2-iodo-HCID 384526—
LösungsmittelBenzeneHCID 241—
Produkt2-(4'-Chloroacetamido-3-iodophenyl) benzothiazoleHCID 1050267871,2%

Reaktionsbedingungen

Temperatur50 °C

Reaktionsschritte

To a solution of 2-(4'-amino-3'-iodophenyl) benzothiazole (DF129) (0.15 g, 0.426 mmol) in benzene (15 ml) was added dropwise chloroacetyl chloride (0.18 g) at room temperature. A yellow precipitate was formed and the resulting mixture was stirred at 50° C. for 30 minutes, and then cooled in an ice-bath. The solid was filtered off, washed with cold benzene and petroleum ether, and dried to give a yellow powder (0.13 g, 71.2%), m.p. 192.1-193.8° C.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS06034246
Quelldatensatzuspto-grants-2000_03
ORD IDord-4e82fcd6e88542cf85eaa0570c499bcf
Quellennotizuspto-grants-2000_03