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HRID 132094Erstellt: 26. Oktober 2026

2-Chloro-1,1-diethoxyethane → Thiazole, 2-[(3,4,4-trifluoro-3-butenyl)thio]-

https://huagongshe.com/reaction/132094

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
Edukt2-Chloro-1,1-diethoxyethaneHCID 12128—
Eduktp-Toluenesulfonic acid monohydrateHCID 521998—
Edukt3,4,4-Trifluoro-3-butenyl dithiocarbamateHCID 11298598—
LösungsmittelAcetic AcidHCID 176—
ProduktThiazole, 2-[(3,4,4-trifluoro-3-butenyl)thio]-HCID 11447455—

Reaktionsbedingungen

Temperatur95 °C

Reaktionsschritte

3 g (14.9 mmol) of 3,4,4-trifluoro-3-butenyl dithiocarbamate in 15 ml of glacial acetic acid are admixed with 2.3 g (15.1 mmol) of chloroacetaldehyde diethyl acetal and 40 mg of p-toluenesulphonic acid monohydrate. The mixture is stirred at 95° C. for 1.5 h and, after cooling to room temperature, is then concentrated by evaporation under reduced pressure. The evaporation residue is taken up in dichloromethane and washed with 1 N sodium hydroxide solution, and the organic phase is removed, dried over Na2SO4 and concentrated by evaporation under reduced pressure. 2.8 g (81.5% of theory; purity by GC/MS: 97.7 area %) of an oil are obtained.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS07385093B2
Quelldatensatzuspto-grants-2008_06
ORD IDord-28481e56ec6a4857bec8f2d2ba7909af
Quellennotizuspto-grants-2008_06