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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 223437Generated: October 25, 2026

Phenacyl bromide → 6,6-Dimethyl-8-Keto-2-Phenyl-5,6,7,8-Tetrahydroimidazo[2,1-b]Benzothiazole

https://huagongshe.com/reaction/223437

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPhenacyl bromideHCID 6259—
Reactant2-Amino-5,5-dimethyl-5,6-dihydro-4H-benzothiazol-7-oneHCID 587874—
SolventChloroformHCID 6212—
Product6,6-Dimethyl-8-Keto-2-Phenyl-5,6,7,8-Tetrahydroimidazo[2,1-b]BenzothiazoleHCID 914349—

Reaction Steps

A 0.08 m. quantity each of 2-amino-5,5-dimethyl-7-keto-4,5,6,7-tetrahydrobenzothiazole and α-bromoacetophenone are mixed in 150 ml. of chloroform and heated at reflux for 4 hours. The slurry is filtered hot and the insoluble intermediate product is suspended in 600 ml. of water containing 25 g. of sodium acetate. This suspension is heated slowly to boil over 21/2 hours, then allowed to cool. The product is filtered off, washed well with water and dried yielding 12.5 g. of product melting at 175°-178° C. and having the structure: ##STR9##

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04354970
Source datasetuspto-grants-1982_10
ORD IDord-d33b617395a44d15bdfce6aea95b21bf
Source noteuspto-grants-1982_10