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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1782527Generated: October 25, 2026

Nitric Acid → 4-Methyl-5-(2-nitrooxy-ethyl)-thiazol-2-ylamine

https://huagongshe.com/reaction/1782527

Reaction equation

Participants

RoleNameHCIDCharge
ReactantNitric AcidHCID 944—
ReactantSulfuric AcidHCID 1118—
ReactantSodium HydroxideHCID 14798—
Reactant2-Amino-4-methyl-5-hydroxyethylthiazoleHCID 150943—
SolventWaterHCID 962—
SolventHexaneHCID 8058—
Product4-Methyl-5-(2-nitrooxy-ethyl)-thiazol-2-ylamineHCID 11557499—

Reaction Conditions

Temperature25 °C

Reaction Steps

Subsequently, 4-methyl-5-(2-nitrooxy-ethyl)-thiazole-2-ylamine was prepared by drop-wise addition of 1.59 grams of nitric acid (70%) to 2.48 grams of cooled sulfuric acid (95-98%) at 0-5° C. over a time period of 20 minutes. Following, 4 grams (0.025 moles) of 2-(2-Amino-4-methyl-thiazol-5-yl)-ethanol were added over a time period of 45 minutes at 0-5° C. After the addition was completed, the reaction mixture was stirred for 3 hours at 25° C., and was then added carefully to 50 ml of cold water. The water solution was turned basic with an aqueous solution of 20% sodium hydroxide and the aqueous phase was extracted with three portions of 75 grams of ethyl acetate. The organic extracts were combined, dried over sodium sulfate, filtered and evaporated to dryness under vacuum. Chromatography of the crude product on silica gel (using a mixture of 8:2 ethyl acetate:hexane as eluent) gave 1.8 grams (35% yield) of the product as orange oil having a purity of 98.5% as determined by gas chromatography.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07498445B2
Source datasetuspto-grants-2009_03
ORD IDord-3827bb123715487491da1dadc3313d18
Source noteuspto-grants-2009_03