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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 56766Erstellt: 24. Oktober 2026

Ammonium Chloride → Tert-butyl 2-(2-methoxyethyl)-1,3-dithiane-2-carboxylate

https://huagongshe.com/de/reaction/56766

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktAmmonium ChlorideHCID 25517—
Edukt1-Iodo-2-methoxyethaneHCID 79136—
EduktPotassium tert-butoxideHCID 23665647—
EduktTert-butyl 1,3-dithiane-2-carboxylateHCID 86007917—
LösungsmittelDimethylformamideHCID 6228—
ProduktTert-butyl 2-(2-methoxyethyl)-1,3-dithiane-2-carboxylateHCID 90060334—

Reaktionsbedingungen

Temperatur0 °C

Reaktionsschritte

10.2 g (46.1 mmol) of tert-butyl 1,3-dithiane-2-carboxylate and 12.0 g (64.5 mmol) of 1-iodo-2-methoxyethane were initially charged in 127 ml of dimethylformamide, the mixture was cooled to 0° C. and 6.21 g (55.3 mmol) of potassium tert-butoxide were added. The resulting reaction mixture was stirred at 0° C. for 1 h and at RT for 16 h. The reaction mixture was added to 1.5 l of a 1:2 mixture of ice and saturated aqueous ammonium chloride solution and extracted three times with 300 ml of diethyl ether. The combined organic phases were dried over magnesium sulphate and filtered, and the solvent was removed under reduced pressure. The crude product was used for the next step without further purification. Yield: 11.1 g (87% of theory)

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS09434690B2
Quelldatensatzuspto-grants-2016_09
ORD IDord-23e59bb0f1e44d93a51a2c618ff37b6d
Quellennotizuspto-grants-2016_09