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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 737151Generated: October 29, 2026

2-Bromo-1-(3-nitrophenyl)ethan-1-one → 2-Amino-4-(3-nitrophenyl)thiazole

https://huagongshe.com/reaction/737151

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-Bromo-1-(3-nitrophenyl)ethan-1-oneHCID 75213—
ReactantSodium AcetateHCID 517045—
ReactantThioureaHCID 2723790—
SolventEthanolHCID 702—
Product2-Amino-4-(3-nitrophenyl)thiazoleHCID 613504—

Reaction Steps

Thiourea (0.31 g, 4.1 mmol) and sodium acetate (0.44 g, 5.3 mmol) were combined in 30 mL of dry ethanol. To this suspension was added 2-bromo-1-(3-nitro-phenyl)-ethanone (1.0 g, 4.1 mmol). Reaction mixture was stirred at room temperature overnight. Reaction mixture was evaporated to dryness to yield 4-(3-nitro-phenyl)-thiazol-2-ylamine, which was used in the next step without any further purification. MS: 222.0 (M+H+).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07595398B2
Source datasetuspto-grants-2009_09
ORD IDord-f7662110da014159a7bae5deff1ab0bd
Source noteuspto-grants-2009_09