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HRID 351797Erstellt: 24. Oktober 2026

Ammonium Chloride → 5-Methoxymethyl-2-(3,4,4-trifluoro-3-butenylthio)oxazole

https://huagongshe.com/de/reaction/351797

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktAmmonium ChlorideHCID 25517—
EduktBromomethyl methyl etherHCID 83093—
Edukt2-(3,4,4-Trifluoro-3-butenylthio)oxazoleHCID 12993958—
EduktButyllithiumHCID 178418339—
LösungsmittelDiethyl EtherHCID 3283—
Produkt5-Methoxymethyl-2-(3,4,4-trifluoro-3-butenylthio)oxazoleHCID 2271464313,2%

Reaktionsschritte

10.40 ml of n-butyl lithium (1.6 M n-hexane solution) were slowly added dropwise to a solution of 3.14 g of 2-(3,4,4-trifluoro-3-butenylthio)oxazole in 40 ml of ether at −70° C. After stirring for 1 hour, a solution of 2.06 g bromomethyl methyl ether in 10 ml ether was added dropwise. After bringing the mixture back to room temperature and stirring for 1 hour, 50 ml of saturated solution of ammonium chloride was added to separate it into an ether layer and an aqueous layer. The aqueous layer was further extracted with ether and together with the separated ether layer it was washed with a saturated sodium chloride water and dried with anhydrous magnesium sulfate. After the solvent was distilled off under reduced pressure, the residue was treated by column chromatography to obtain 0.5 g of 5-methoxymethyl-2-(3,4,4-trifluoro-3-butenylthio)oxazole (yield 13%). n20D=1.4705.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS06743814B2
Quelldatensatzuspto-grants-2004_06
ORD IDord-5c93f45f4f014b839b8462967fe84277
Quellennotizuspto-grants-2004_06