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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 325381Erstellt: 24. Oktober 2026

Acetic Anhydride → Ethyl 2-formamidothiazol-4-acetate

https://huagongshe.com/de/reaction/325381

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktAcetic AnhydrideHCID 7918—
Edukt4-Thiazoleacetic acid, 2-amino-, ethyl esterHCID 104454—
EduktHCID 178470764HCID 178470764—
LösungsmittelFormic AcidHCID 284—
ProduktEthyl 2-formamidothiazol-4-acetateHCID 688091—

Reaktionsschritte

To acetic anhydride (384 ml.) was dropwise added formic acid (169.2 ml.) over 15 to 20 minutes under cooling below 35° C., and the mixture was stirred for 1 hour at 55° to 60° C. To the mixture was added ethyl 2-(2-amino-1,3-thiazol-4-yl)acetate, which can be represented as ethyl 2-(2-imino-2,3-dihydro-1,3-thiazol-4-yl)acetate, (506 g.) over 15 to 20 minutes under ice-cooling and stirring, and then the mixture was stirred for 1 hour at room temperature. After the reaction, the solvents were distilled off. To the residue was added diisopropyl ether (2500 ml.), and the mixture was stirred for 1 hour at room temperature. The precipitates were collected by filtration, washed with diisopropyl ether and then dried to give ethyl 2-(2-formylamino-1,3-thiazol-4-yl)acetate, which can be represented as ethyl 2-(2-formylimino-2,3-dihydro-1,3-thiazol-4-yl)acetate, (451.6 g.), mp. 125° to 126° C. The remaining filtrate was concentrated, and the residue was washed with diisopropyl ether (500 ml.) and then dried to give further the same object compound (78.5 g.).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS04440766
Quelldatensatzuspto-grants-1984_04
ORD IDord-dea44d98d1cb4878a1f1c7a59bcfe69d
Quellennotizuspto-grants-1984_04