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HRID 249276作成日:2026年10月24日

4-Hydroxybenzaldehyde → 4-[[6-(Diethylamino)hexyl]oxy]benzaldehyde

https://huagongshe.com/ja/reaction/249276

反応式

関与物質

役割名称HCID仕込み量
反応物4-HydroxybenzaldehydeHCID 126—
反応物TriphenylphosphineHCID 11776—
反応物ethyl N-ethoxycarbonyliminocarbamateHCID 220568—
反応物6-(Diethylamino)-1-hexanolHCID 245054—
溶媒TetrahydrofuranHCID 8028—
生成物4-[[6-(Diethylamino)hexyl]oxy]benzaldehydeHCID 1976101364.3%

反応手順

A mixture of 2.17 g of 6-diethylamino-1-hexanol (J. Chem. Soc. 1942, 428), 1.52 g of 4-hydroxy-benzaldehyde and 3.3 g of triphenylphosphine in 100 ml of tetrahydrofuran was treated slowly at 20° with a solution of 1.97 g of diethyl azodicarboxylate. After the dropwise addition the mixture was stirred at room temperature for a further 5 hours. The reaction mixture was then evaporated in a rotary evaporator. The residue was chromatographed on 400 g of neutral aluminium oxide (activity grade III) with hexane:ethyl acetate (7:3). There were obtained 2.22 g (64%) of 4-[[6-(diethylamino)hexyl]oxy]benzaldehyde as a yellowish oil.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US05214046
出典データセットuspto-grants-1993_05
ORD IDord-187ac58ef0194af39d7fd19eefd6b4ef
出典メモuspto-grants-1993_05