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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 737171Generated: October 25, 2026

1,4-Diacetylbenzene → 1-[4-(2-Amino-thiazol-4-yl)-phenyl]-ethanone

https://huagongshe.com/reaction/737171

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1,4-DiacetylbenzeneHCID 13888—
ReactantBromineHCID 24408—
ReactantCarbonyl bromideHCID 79057—
ReactantSodium AcetateHCID 517045—
ReactantThioureaHCID 2723790—
SolventAcetic AcidHCID 176—
SolventEthanolHCID 702—
Product1-[4-(2-Amino-thiazol-4-yl)-phenyl]-ethanoneHCID 86616431—

Reaction Steps

A solution of 1-(4-Acetyl-phenyl)-ethanone (8.1 g, 5 mmol), in HOAc (50 mL) at 60° C. was treated with bromine (1 eq., 0.26 mL) dropwise over 10 minutes. After 5 more minutes the reaction was cooled, the acetic acid was removed, ethyl acetate (50 mL) was added and then removed to get drive off the remainder of the acetic acid. The crude bromo ketone was then dissolved in ethanol (30 mL) with NaOAc (1.1 g) and thiourea (1 eq., 375 mg) was added. The suspension was stirred at room temperature for 15 hours. The solvents were removed and the resulting mixture was redissolved in 5 ml of 90% DMF, 10% water with 0.1% TFA and purified by reverse phase HPLC to give the product. MS: 219.1 (M+H−).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07595398B2
Source datasetuspto-grants-2009_09
ORD IDord-bf1e3eb4baff409c84040f25d0325913
Source noteuspto-grants-2009_09