Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 737168Generated: October 26, 2026

4-Acetylbenzoic Acid → 4-(2-Amino-1,3-thiazol-4-yl)benzoic acid

https://huagongshe.com/reaction/737168

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-Acetylbenzoic AcidHCID 11470—
ReactantBromineHCID 24408—
ReactantCarbonyl bromideHCID 79057—
ReactantSodium AcetateHCID 517045—
ReactantThioureaHCID 2723790—
SolventAcetic AcidHCID 176—
SolventEthanolHCID 702—
Product4-(2-Amino-1,3-thiazol-4-yl)benzoic acidHCID 613179—

Reaction Steps

A solution of 4-acetyl-benzoic acid (10 g, 61 mmol), in HOAc (400 mL) at 55° C. was treated with bromine (1 eq., 3.12 mL) dropwise over 10 minutes. After 90 minutes the reaction was cooled, the acetic acid was removed, ethyl acetate (50 mL) was added and then removed to get rid of the remainder of the acetic acid. The crude bromo ketone was then dissolved in ethanol (200 mL) with NaOAc (12 g) and thiourea (1 eq. 4.4 g) was added. The suspension was stirred at room temperature for 15 hours. The solvents were removed and the solids washed with water (3×100 mL) then ether:ethanol (4:1, 3×100 mL) and dried to give the product as a tan solid. MS: 221.2 (M+H+).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07595398B2
Source datasetuspto-grants-2009_09
ORD IDord-d29e033db8d04bd3b35694af9be5cf39
Source noteuspto-grants-2009_09