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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 30653Generated: October 26, 2026

1-Bromo-2-butanone → 4-Ethyl-2-[2-(4-nitrophenyl)ethyl]-1,3-thiazole

https://huagongshe.com/reaction/30653

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1-Bromo-2-butanoneHCID 13156—
Reactant3-(4-Nitrophenyl)propanethioamideHCID 82673146—
Solventtert-ButanolHCID 6386—
Product4-Ethyl-2-[2-(4-nitrophenyl)ethyl]-1,3-thiazoleHCID 6920925495%

Reaction Steps

A mixture of 3-(4-nitrophenyl)propanethioamide (1.25 g), 1-bromo-2-butanone (0.98 g) and tert-butanol (30 mL) was heated under reflux for 30 min. The reaction mixture was concentrated, and saturated aqueous sodium hydrogen carbonate was added to the residue. The mixture was extracted with ethyl acetate. The organic layer was washed with saturated brine, dried over anhydrous magnesium sulfate and concentrated. The residue was subjected to silica gel column chromatography to give 4-ethyl-2-[2-(4-nitrophenyl)ethyl]-1,3-thiazole as a yellow oil (1.48 g, yield 95%) from a fraction eluted with hexane-ethyl acetate (4:1-2:1, v/v).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07423159B2
Source datasetuspto-grants-2008_09
ORD IDord-bce00eac5075431fb0aeab203b251a1e
Source noteuspto-grants-2008_09