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HRID 1445765Erstellt: 24. Oktober 2026

1,3-Dithiane → 2-(4-Bromo-phenyl)-4-(2-[1,3]dithian-2-yl-ethyl)-5-methyl-oxazole

https://huagongshe.com/de/reaction/1445765

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
Edukt1,3-DithianeHCID 10451—
Edukt2(1H)-Pyrimidinone, tetrahydro-1,3-dimethyl-HCID 81646—
Edukt1,2-DithianeHCID 136335—
Edukt2-(4-Bromo-phenyl)-4-(2-iodo-ethyl)-5-methyl-oxazoleHCID 58951394—
EduktButyllithiumHCID 178418339—
LösungsmittelWaterHCID 962—
LösungsmittelTetrahydrofuranHCID 8028—
Produkt2-(4-Bromo-phenyl)-4-(2-[1,3]dithian-2-yl-ethyl)-5-methyl-oxazoleHCID 8609668466%

Reaktionsbedingungen

Temperatur-78 °C

Reaktionsschritte

Add a cold (−78° C.) solution of 2-(4-bromo-phenyl)-4-(2-iodo-ethyl)-5-methyl-oxazole (See Intermediate 30) (1.05 g, 2.67 mmol) in 15 mL THF to a cold (−78° C.) solution of dithiane anion [Preparation: Add n-BuLi (7.5 mL, 12 mmol, 1.6M in hexanes) to a −20° C. solution of 1,3-dithiane (1.92 g, 15.9 mmol) in 25 mL THF. Stir 20 min at −78° C. and add 1,3-dimethyl-3,4,5,6-tetrahydro-2(1H)-pyrimidinone (DMPU, 4.03 g, 31.4 mmol).] Stir the reaction mixture at −78° C. for 15 min. Add water and warm to room temperature. Add dichloromethane, and separate the layers. Dry the crude organic extracts over MgSO4, filter and concentrate. Purify on silica gel 0-10% EtOAc/Hexanes to give 2-(4-bromo-phenyl)-4-(2-[1,3]dithian-2-yl-ethyl)-5-methyl-oxazole (0.672 g, 66%). MS (m/e): 384 (M+1).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS07666871B2
Quelldatensatzuspto-grants-2010_02
ORD IDord-283878666e17431bac2c7bdebad67a41
Quellennotizuspto-grants-2010_02