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HRID 11119作成日:2026年10月23日

4-(Benzyloxy)-3-methoxybenzaldehyde → Methyl-2-azido-3-[4'-(benzyloxy)-3'-methoxyphenyl]prop-2-enoate

https://huagongshe.com/ja/reaction/11119

反応式

関与物質

役割名称HCID仕込み量
反応物4-(Benzyloxy)-3-methoxybenzaldehydeHCID 75506—
反応物Methyl 2-azidoacetateHCID 4020482—
反応物SodiumHCID 5360545—
反応物Sodium MethoxideHCID 10942334—
溶媒MethanolHCID 887—
生成物Methyl-2-azido-3-[4'-(benzyloxy)-3'-methoxyphenyl]prop-2-enoateHCID 7239054073%

反応条件

温度0 °C

反応手順

A solution of the 4-Benzyloxy-3-methoxy-benzaldehyde (12.0 g, 49.6 mmol) and methyl azidoacetate (23 g, 0.200 mol) in methanol (50 mL) was added over 30 min to a cooled (ice-salt bath) solution of sodium methoxide which had been prepared from addition of methanol (80 mL) to sodium (3.4 g, 0.149 mol). The reaction mixture was stirred at 0° C. for 45 min, during this time a thick cream precipitate formed, and then stood in the freezer overnight. Ice-cold water was added and the precipitate was removed by filtration and dried to give methyl-2-azido-3-[4′-(benzyloxy)-3′-methoxyphenyl]prop-2-enoate (55) (12.2 g, 73%) which was used in the next step without purification.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07094798B1
出典データセットuspto-grants-2006_08
ORD IDord-d9e8ac3d46b14af1810494a565aed42a
出典メモuspto-grants-2006_08