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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 16215Erstellt: 24. Oktober 2026

2-Butene-1,4-diol → 4-(tert-Butyl-diphenyl-silanyloxy)-but-2-en-1-ol

https://huagongshe.com/de/reaction/16215

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
Edukt2-Butene-1,4-diolHCID 8065—
EduktSodium hydrideHCID 24758—
Edukttert-ButyldiphenylchlorosilaneHCID 94078—
LösungsmittelTetrahydrofuranHCID 8028—
Produkt4-(tert-Butyl-diphenyl-silanyloxy)-but-2-en-1-olHCID 66656949—

Reaktionsschritte

NaH (3 g, 75 mmol, 60% in oil) was added portion-wise to a stirred and cooled (0° C.) solution of but-2-ene-1,4-diol (6 g, 68.09 mmol) in dry tetrahydrofuran (250 mL). After the addition, the mixture was allowed to warm to room temperature and stirred for another two hours. The resulting white mixture was then cooled (0° C.) and tert-butyl-chlorodiphenylsilane (15.7 mL, 61.28 mmol) was added drop wise. After twenty minutes, the cooling bath was removed and the mixture was allowed to stir overnight at room temperature. Saturated NH4Cl was poured into the reaction mixture and the reaction was partitioned with diethyl ether (200 mL). The organic layer was washed with brine, dried (MgSO4), and filtered. The resulting oil was used in the following step without further purification.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS07737137B2
Quelldatensatzuspto-grants-2010_06
ORD IDord-cacae96a195b4eb7a82169604af3d677
Quellennotizuspto-grants-2010_06