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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1923607Generated: October 29, 2026

Sulfuric Acid → 2-[(E)-2-(3-Butyl-5-methyl-isoxazol-4-yl)-vinyl]-4-methyl-thiazole-5-carboxylic acid methyl ester

https://huagongshe.com/reaction/1923607

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSulfuric AcidHCID 1118—
ReactantSodium HydroxideHCID 14798—
Reactant2-[2-(3-Butyl-5-methyl-isoxazol-4-yl)-2-hydroxy-ethyl]-4-methyl-thiazole-5-carboxylic acid methyl esterHCID 66643697—
SolventEthyl AcetateHCID 8857—
Product2-[(E)-2-(3-Butyl-5-methyl-isoxazol-4-yl)-vinyl]-4-methyl-thiazole-5-carboxylic acid methyl esterHCID 6664365194.1%

Reaction Conditions

Temperature90 °C

Reaction Steps

Concentrated sulfuric acid (85 mL) was added to 2-[2-(3-butyl-5-methyl-isoxazol-4-yl)-2-hydroxy-ethyl]-4-methyl-thiazole-5-carboxylic acid methyl ester (9.0 g, 26.6 mmol) then the mixture was heated at 90° C. for 2 h. The solution was carefully dropped into 2N sodium hydroxide (1580 mL) and ethyl acetate (100 mL) saturated sodium bicarbonate was added until pH 10 was reached. The reaction mixture was extracted with ethyl acetate then the combined organic extracts were dried, filtered and concentrated, to give the title compound (8.02 g, 94%) as a yellow oil that was used directly without further purification. MS: m/e=321.2 [M+H]+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08178522B2
Source datasetuspto-grants-2012_05
ORD IDord-31d7e03547d943c7b4368c20fe4e0c57
Source noteuspto-grants-2012_05