Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 635844Generated: October 30, 2026

Ethyl Acetate → HCID 21256452, compound

https://huagongshe.com/reaction/635844

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthyl AcetateHCID 8857—
ReactantSodium DithioniteHCID 24489—
ReactantSodium BicarbonateHCID 516892—
ReactantHCID 86756425HCID 86756425—
SolventWaterHCID 962—
SolventTolueneHCID 1140—
ProductHCID 21256452HCID 21256452—

Reaction Steps

A solution of 2-(4-Bromophenyl)-E-ethenylimidazo[2,1-b]thiazol-5-yl methanone (Formula B-9) (1.04 g) in toluene (160 mL) was treated with a solution prepared by dissolving Na2S2O4 (14.4 g) in water (220 mL), adding sodium bicarbonate (15.6 g) and Aliquot®336 (0.41 mL). The vigorously stirred suspension was heated at 100° for 85 hours, diluted with ethyl acetate and partitioned. The extract was washed with saline solutions, dried and evaporated to a viscous residue. The residue was chromatographed on silica gel and product was eluted with 4:1 hexane:ethyl acetate to provide 2-(4-Bromophenylethyl)-3-methylimidazo[2,1-b]thiazol-5-yl methanone (Formula B-10) (0.220 g). An aliquot was crystallized from isopropanol to yield pure 2-(4-Bromophenylethyl)-3-methylimidazo[2,1-b]thiazol-5-yl methanone (Formula B-10), m.p, 113-115°.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06191124B1
Source datasetuspto-grants-2001_02
ORD IDord-aee9c18402f947ac99b657d170cdd747
Source noteuspto-grants-2001_02