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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1094826Generated: October 25, 2026

Nitric Acid → 2-Ethyl-4-methyl-5-(2-nitrooxy-ethyl)-thiazole

https://huagongshe.com/reaction/1094826

Reaction equation

Participants

RoleNameHCIDCharge
ReactantNitric AcidHCID 944—
ReactantSulfuric AcidHCID 1118—
ReactantSodium HydroxideHCID 14798—
Reactant2-(2-Ethyl-4-methyl-thiazol-5-yl)-ethanolHCID 18440824—
SolventWaterHCID 962—
SolventHexaneHCID 8058—
Product2-Ethyl-4-methyl-5-(2-nitrooxy-ethyl)-thiazoleHCID 1168716458%

Reaction Conditions

Temperature2.5 °C

Reaction Steps

Fifteen (15) ml of nitric acid of (85-90%) were added dropwise to 15 ml of sulfuric acid (95-98%) over a time period of 20 minutes while keeping the temperature at 0-5° C. After 2 hours, 14.3 grams (83.60 mmol) of 2-ethyl-4-methyl-5-thiazoleethanol, prepared as described above, were added, while the temperature was still maintained at 0-5° C., the reaction mixture was stirred for 2 hours at the same temperature, and was then poured carefully onto 125 ml of cold water. The water solution was made basic with a 20% aqueous solution of sodium hydroxide and the aqueous phase was extracted with three portions of 75 grams of dichloromethane. The extracts were combined and dried over sodium sulfate, filtered and evaporated to dryness. Chromatography of the crude product on silica gel (using a mixture of 75:25 ethyl acetate:hexane as an eluent) yielded 10.5 grams (58% yield) of colorless liquid having a purity of 98%, as determined by gas chromatography.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08134010B2
Source datasetuspto-grants-2012_03
ORD IDord-52a779a2a4224834a9e71c53a830475c
Source noteuspto-grants-2012_03