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HRID 652800作成日:2026年10月25日

Chloromethyl Methyl Ether → 3-Benzyloxy-4-methoxybenzaldehyde

https://huagongshe.com/reaction/652800

反応式

関与物質

役割名称HCID仕込み量
反応物Chloromethyl Methyl EtherHCID 7864—
反応物Sodium hydrideHCID 24758—
反応物3-Benzyloxy-4-hydroxybenzaldehydeHCID 11020635—
溶媒WaterHCID 962—
溶媒DimethylformamideHCID 6228—
生成物3-Benzyloxy-4-methoxybenzaldehydeHCID 80671—

反応手順

A solution of 300 g of 3-benzyloxy-4-hydroxybenzaldeyde (obtained as described in example 62) in 600 ml of dimethylformamide was added to a suspension of 34.6 g of sodium hydride in 346 ml of dimethylformamide under stirring in nitrogen atmosphere. After complete dissolution of sodium hydride 116 g of chloromethyl methyl ether were added; stirring was continued for 30 minutes. The mixture was then diluted with water and extracted with ethyl ether. The combined organic phase was dried over sodium sulfate, filtered and evaporated. The residue was distilled (b.p. 178°-183° C./0.1 mm Hg) to give 3-benzyloxy-4-methoxybenzaldehyde, m.p. 30° C. (from petroleum ether, b.p. 30°-70° C.).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US04673671
出典データセットuspto-grants-1987_06
ORD IDord-95efb3875a0543a7a9361ee7cf4d6162
出典メモuspto-grants-1987_06