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HRID 339662作成日:2026年10月26日

Imidazole → 8-(Tert-butyldimethylsilyloxy)quinoline-2-carbaldehyde

https://huagongshe.com/reaction/339662

反応式

関与物質

役割名称HCID仕込み量
反応物ImidazoleHCID 795—
反応物tert-Butyldimethylsilyl chlorideHCID 28928—
反応物8-Hydroxy-2-quinolinecarboxaldehydeHCID 599342—
溶媒DichloromethaneHCID 6344—
生成物8-(Tert-butyldimethylsilyloxy)quinoline-2-carbaldehydeHCID 5856708283%

反応手順

8-Hydroxyquinoline-2-carbaldehyde (5.00 g, 28.9 mmol) and imidazole (4.32 g, 63.5 mmol) were dissolved in DCM (50 mL) under N2. The reaction mixture was cooled to 0° C. after which time tert-butylchlorodimethylsilane (4.94 g, 31.8 mmol) was added. After stirring for 16 hours at ambient temperature, the reaction mixture was partitioned between DCM and H2O. The organic layer was washed with H2O and aqueous saturated NaHCO3, dried over Na2SO4, filtered and concentrated under reduced pressure to afford an orange oil. The residue was purified via flash column chromatography (10:1 Hexane/EtOAc) to provide 6.85 g (83%) of desired product as a yellow/orange oil.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08895550B2
出典データセットuspto-grants-2014_11
ORD IDord-8b72e96bd29f41a38b067d733efbf1ca
出典メモuspto-grants-2014_11