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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 891Erstellt: 23. Oktober 2026

Hydrochloric Acid → 4-(4-tert-Butyldiphenylsilyloxymethyl-phenyl)butyraldehyde

https://huagongshe.com/de/reaction/891

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktHydrochloric AcidHCID 313—
EduktImidazoleHCID 795—
EduktPotassium CarbonateHCID 11430—
Edukttert-ButyldiphenylchlorosilaneHCID 94078—
Edukt2-[3-(4-tert-Butyldiphenylsilyloxymethylphenyl)propyl]-[1,3]-dioxolaneHCID 19694134—
LösungsmittelTetrahydrofuranHCID 8028—
Produkt4-(4-tert-Butyldiphenylsilyloxymethyl-phenyl)butyraldehydeHCID 1969413142,8%

Reaktionsschritte

To a solution of 5.5 g (11.9 mmol) of the dioxolane 171 in 40 mL of THF at room temperature was added 40 mL of 4.0N HCl and the resulting solution was allowed to stir for 1 h. The mixture was neutralized with solid K2CO3, extracted with ethyl acetate and concentrated. The crude mixture was dissolved into 25 mL of CH2Cl2 to which was added 600 mg (8.8 mmol) of imidazole and 1.9 mL (7.3 mmol) of tert-butylchlorodiphenyl silane. The resulting mixture was allowed to stir overnight at room temperature and was then poured into 0.5N HCl and extracted with ethyl acetate. The organics were dried over MgSO4, filtered and concentrated. Flash chromatography (elution with 8% ethyl acetate in hexane) gave 2.12 g of the aldehyde 172 as an oil. 1H NMR consistent with the product.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS05723459
Quelldatensatzuspto-grants-1998_03
ORD IDord-991308a13d764cc0817ac696051b408e
Quellennotizuspto-grants-1998_03