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HRID 891作成日:2026年10月23日

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

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

反応式

関与物質

役割名称HCID仕込み量
反応物Hydrochloric AcidHCID 313—
反応物ImidazoleHCID 795—
反応物Potassium CarbonateHCID 11430—
反応物tert-ButyldiphenylchlorosilaneHCID 94078—
反応物2-[3-(4-tert-Butyldiphenylsilyloxymethylphenyl)propyl]-[1,3]-dioxolaneHCID 19694134—
溶媒TetrahydrofuranHCID 8028—
生成物4-(4-tert-Butyldiphenylsilyloxymethyl-phenyl)butyraldehydeHCID 1969413142.8%

反応手順

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.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US05723459
出典データセットuspto-grants-1998_03
ORD IDord-991308a13d764cc0817ac696051b408e
出典メモuspto-grants-1998_03