Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1636563Generated: October 25, 2026

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

https://huagongshe.com/reaction/1636563

Reaction equation

Participants

RoleNameHCIDCharge
ReactantChloroacetyl chlorideHCID 6577—
ReactantBenzenamine, 4-(2-benzothiazolyl)-2-iodo-HCID 384526—
SolventBenzeneHCID 241—
Product2-(4'-Chloroacetamido-3-iodophenyl) benzothiazoleHCID 1050267871.2%

Reaction Conditions

Temperature50 °C

Reaction Steps

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.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06034246
Source datasetuspto-grants-2000_03
ORD IDord-4e82fcd6e88542cf85eaa0570c499bcf
Source noteuspto-grants-2000_03