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HRID 24408作成日:2026年10月26日

Triphenylphosphine → 3-Tert-butyl-4-(2-morpholin-4-ylethoxy)benzaldehyde

https://huagongshe.com/reaction/24408

反応式

関与物質

役割名称HCID仕込み量
反応物TriphenylphosphineHCID 11776—
反応物2-MorpholinoethanolHCID 61163—
反応物3-(tert-Butyl)-4-hydroxybenzaldehydeHCID 3017618—
反応物Diethyl azodicarboxylateHCID 5462977—
溶媒TetrahydrofuranHCID 8028—
生成物3-Tert-butyl-4-(2-morpholin-4-ylethoxy)benzaldehydeHCID 2257107244%

反応手順

Triphenylphosphine (5.89 g, 22.44 mmol) was added to a solution of 3-tert-butyl-4-hydroxybenzaldehyde (4 g, 22.44 mmol) in tetrahydrofuran (40 ml), followed by addition of 2-hydroxyethylmorpholine (2.94 g, 22.44 mmol) and then the dropwise addition of diethylazodicarboxylate (3.91 g, 22.44 mmol). The mixture was allowed to stir at room temperature for 3 days. The reaction was concentrated under reduced pressure and partitioned between 2N hydrochloric acid (200 ml) and ethyl acetate (150 ml). The aqueous layer was extracted with ethyl acetate (2×150 ml), basified to pH 9 with solid sodium bicarbonate, saturated with solid sodium chloride and extracted with ethyl acetate (3×150 ml). The combined organic layers were dried over magnesium sulfate and concentrated to afford 2.8 g (44%) of 3-tert-butyl-4-(2-morpholin-4-ylethoxy)benzaldehyde as a yellowish oil.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US06855730B2
出典データセットuspto-grants-2005_02
ORD IDord-b74638abcaa1446e966896a2dd908b5f
出典メモuspto-grants-2005_02