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HRID 22602作成日:2026年10月26日

4-Pyrrolidinopyridine → Benzaldehyde, 3-[[[(1,1-dimethylethyl)diphenylsilyl]oxy]methyl]-

https://huagongshe.com/reaction/22602

反応式

関与物質

役割名称HCID仕込み量
反応物4-PyrrolidinopyridineHCID 75567—
反応物tert-ButyldiphenylchlorosilaneHCID 94078—
反応物3-(Hydroxymethyl)benzaldehydeHCID 13131455—
溶媒DichloromethaneHCID 6344—
溶媒TriethylamineHCID 8471—
生成物Benzaldehyde, 3-[[[(1,1-dimethylethyl)diphenylsilyl]oxy]methyl]-HCID 10883279—

反応手順

To a solution of 3-hydroxymethylbenzaldehyde (step 1) (3 g) in methylene chloride (15 mL) and triethylamine (4.1 mL) was slowly added t-butylchlorodiphenyl silane (8 mL). Finally, a few mgs of 4-pyrrolidinopyridine was added as a catalyst. The reaction mixture was stirred overnight at room temperature (R.T.). The solution was quenched with 25% ammonium acetate and extracted with ethyl acetate, which was washed with brine (2×), dried over sodium sulfate, filtered and evaporated to dryness. Purification by flash chromatography, using 4% ethyl acetate in hexane afforded the title compound.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US05428171
出典データセットuspto-grants-1995_06
ORD IDord-1cffddb7e50e4d50a76e4abb31db29ea
出典メモuspto-grants-1995_06