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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 52744Erstellt: 23. Oktober 2026

Isoamyl Nitrite → Ethyl thiazole-5-carboxylate

https://huagongshe.com/de/reaction/52744

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktIsoamyl NitriteHCID 8053—
Edukt2-Amino-thiazole-5-carboxylic acid ethyl esterHCID 314628—
LösungsmittelDimethylformamideHCID 6228—
LösungsmittelTetrahydrofuranHCID 8028—
ProduktEthyl thiazole-5-carboxylateHCID 459108—

Reaktionsbedingungen

Temperatur25 °C

Reaktionsschritte

A solution of 2-amino-5-(ethoxycarbonyl)thiazole (50 g, 0.29 mmol) in a mixture of DMF (83 mL) and THF (317 mL) was added dropwise over 87 minutes to a stirred 41° C. solution of isoamyl nitrite (59 mL, 0.44 mol) in DMF (130 mL). A maximum temperature of 60° C. was observed during the exothermic addition. After another 40 minutes the THF was removed under vacuum at 45° C. The concentrated DMF solution was cooled to 25° C. and diluted with toluene (420 mL) and water (440 mL). The toluene layer was extracted with 3×120 mL water, then dried with Na2SO4 (50 g) for 1 hour. After filtration the toluene layer was stripped on a rotary evaporator at 50° C. bath temperature, then on a vacuum pump at 21° C. The crude residue containing the title compound weighed 65.6 g. This material was used directly in the next step. A sample of similarly prepared material was purified by column chromatography to give a yellow oil. 1H NMR (CDCl3) δ8.95 (s, 1H), 8.51 (s, 1H), 4.39 (q, 2H), 1.40 (t, 3H). 13C NMR (CDCl3) δ161.0, 157.9 148.6, 129.8, 61.6, 14.1.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS05616720
Quelldatensatzuspto-grants-1997_04
ORD IDord-9e83b0f445f0431b8d4f47246aeea569
Quellennotizuspto-grants-1997_04