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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 70262Generated: October 28, 2026

Ammonium Hydroxide → 2-(4-Hydroxyphenyl)-1,3-thiazole-4-carboxamide

https://huagongshe.com/reaction/70262

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAmmonium HydroxideHCID 14923—
ReactantChloro-N,N-dimethylformiminium chlorideHCID 77311—
Reactant2-(4-Hydroxyphenyl)-1,3-thiazole-4-carboxylic acidHCID 135767897—
SolventTetrahydrofuranHCID 8028—
Product2-(4-Hydroxyphenyl)-1,3-thiazole-4-carboxamideHCID 136388558—

Reaction Conditions

Temperature0 °C

Reaction Steps

2-(4-Hydroxyphenyl)-1,3-thiazole-4-carboxylic acid (0.835 g, 3.77 mmol) was dissolved in 20 ml of dry tetrahydrofuran and cooled to 0° C. (Chloromethylene)dimethylammonium chloride (0.58 g, 4.53 mmol) was added in one portion. The mixture was stirred at 0° C. for 5 h. 28% Ammonium hydroxide aqueous solution (5 ml) was added, and the reaction mixture was stirred for 15 h at the room temperature. The organic solvent was removed in vacuo and the residue was partitioned between ethyl acetate and saturated sodium carbonate solution. The organic layer was separated and the aqueous phase was extracted twice with ethyl acetate. The combined extracts were washed with brine, dried over magnesium sulfate and concentrated in vacuo. The residue was purified by silica gel column chromatography (0 to 10% methanol in dichloromethane) to give the title compound as beige solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08822518B2
Source datasetuspto-grants-2014_09
ORD IDord-ca1fb5a0ce614dceb9756c153a95f967
Source noteuspto-grants-2014_09