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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1257384Generated: November 1, 2026

2-Oxobutanoic Acid → Methyl 2-amino-5-methyl-1,3-thiazole-4-carboxylate

https://huagongshe.com/reaction/1257384

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-Oxobutanoic AcidHCID 58—
ReactantAmmoniaHCID 222—
ReactantMethanolHCID 887—
ReactantThionyl ChlorideHCID 24386—
ReactantBromineHCID 24408—
ReactantThioureaHCID 2723790—
SolventDiethyl EtherHCID 3283—
ProductMethyl 2-amino-5-methyl-1,3-thiazole-4-carboxylateHCID 113280123%

Reaction Steps

Under a nitrogen atmosphere at 0° C., to a solution of 2-oxobutyric acid (12 g, 120 mmol) in methanol was added thionyl chloride (40 mL, 330 mmol), and the mixture was stirred at the same temperature for 3 hr. The solvent was evaporated under reduced pressure. Under a nitrogen atmosphere at 0° C., to a solution (50 mL) of the residue in diethyl ether was slowly added dropwise a solution (50 mL) of bromine (10 g, 130 mmol) in diethyl ether, and the mixture was stirred overnight while allowing the mixture to spontaneously warm. The solvent was evaporated under reduced pressure. An aqueous solution (120 mL) of the residue and thiourea (6.3 g, 83 mmol) was heated under reflux for 3 hr, and cooled to room temperature. The reaction mixture was neutralized with 20% aqueous ammonia solution. The resulting crude title compound was collected by filtration, washed with water to give the title compound (3.3 g, 23%) as a colorless solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08461348B2
Source datasetuspto-grants-2013_06
ORD IDord-105b28fe59eb47fcab998e5043e04d93
Source noteuspto-grants-2013_06