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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1697256Erstellt: 25. Oktober 2026

2-Bromothiazole → HCID 67269896, Verbindung

https://huagongshe.com/reaction/1697256

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
Edukt2-BromothiazoleHCID 76430—
Edukt(NE,S)-N-[(2S)-2,3-bis[[tert-butyl(dimethyl)silyl]oxy]propylidene]-2-methylpropane-2-sulfinamideHCID 44239381—
EduktButyllithiumHCID 178418339—
LösungsmittelDiethyl EtherHCID 3283—
ProduktHCID 67269896HCID 6726989683%

Reaktionsschritte

A solution of 2-bromothiazole (7.9 ml, 89 mmol) in 200 mL ether was cooled to −78° C. and treated with a solution of n-butyllithium (36 ml, 89 mmol) (2.5N in hexanes). After stirring for 30 minutes the reaction mixture was slowly added to a cooled (−78° C.) suspension of (S,E)-N—((S)-2,3-bis(tert-butyldimethylsilyloxy)propylidene)-2-methylpropane-2-sulfinamide (25.000 g, 59 mmol) in 100 mL ether. The reaction mixture was allowed to stir at −78° C. for one hour. The reaction mixture was quenched with MeOH and saturated NH4Cl solution. The organic solution was washed with water, brine, dried over MgSO4 and concentrated in vacuo. Purification of the crude residue by column chromatography gave (S)—N-((1R,2S)-2,3-bis(tert-butyldimethylsilyloxy)-1-(thiazol-2-yl)propyl)-2-methylpropane-2-sulfinamide (24.81 g, 83% yield).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS08163909B2
Quelldatensatzuspto-grants-2012_04
ORD IDord-94bd15697fa24e409acd93184e48aa52
Quellennotizuspto-grants-2012_04