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HRID 341673Erstellt: 24. Oktober 2026

Hydrochloric Acid → HCID 68733026, Verbindung

https://huagongshe.com/de/reaction/341673

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktHydrochloric AcidHCID 313—
EduktChloroformHCID 6212—
Edukt2,2,6,6-Tetramethylthiopyran-3,5-dioneHCID 15650165—
EduktHCID 178476529HCID 178476529—
Katalysator4-(Dimethylamino)pyridineHCID 14284—
LösungsmittelTolueneHCID 1140—
ProduktHCID 68733026HCID 6873302640,9%

Reaktionsbedingungen

Temperatur80 °C

Reaktionsschritte

2,2,6,6-Tetramethylthiopyran-3,5-dione (10 g, 0.053 mol) (described in Helvetica Chimica Acta, 1992, 75(7), 2265-69) and 4-dimethylaminopyridine (32 g, 0.26 mol) are added to a mixture of chloroform (200 ml) and toluene (50 ml). The reaction mixture is flushed with nitrogen for 15 minutes at ambient temperature. 4-Bromo-2-ethylphenyllead triacetate (34 g, 0.06 mol) is added in one portion and the reaction mixture is stirred and heated to 80° C. (pre-heated oil bath) under an atmosphere of nitrogen for 1 hour. The reaction mixture is cooled to room temperature, acidified to pH 1 with 2N aqueous hydrochloric acid, filtered through a plug of diatomaceous earth and the two phases are separated. The aqueous phase is extracted with dichloromethane (2×100 ml). The organic phases are combined, washed with water, and dried over anhydrous sodium sulfate. The mixture is filtered, and the filtrate is evaporated under reduced pressure. The residue is purified by column chromatography on silica gel to give 4-(4-bromo-2-ethylphenyl)-2,2,6,6-tetramethylthiopyran-3,5-dione as a white solid (8 g).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS08895761B2
Quelldatensatzuspto-grants-2014_11
ORD IDord-2c6339ad292648158a10cbb0d68069b5
Quellennotizuspto-grants-2014_11