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HRID 734166作成日:2026年10月24日

Ethyl vinyl ether → 6-(1-Ethoxy ethoxy)-2-naphthaldehyde

https://huagongshe.com/ja/reaction/734166

反応式

関与物質

役割名称HCID仕込み量
反応物Ethyl vinyl etherHCID 8023—
反応物Benzenesulfonic acid, 4-methyl-, compd. with pyridine (1:1)HCID 466102—
反応物6-Hydroxy-2-naphthaldehydeHCID 2764110—
触媒Ethyl vinyl etherHCID 8023—
溶媒Ethyl AcetateHCID 8857—
生成物6-(1-Ethoxy ethoxy)-2-naphthaldehydeHCID 2313575973%

反応手順

In a 500 mL three neck flask, equipped with a magnetic stirrer, an addition funnel, and a reflux condenser, were charged 25 g of HNAL (0.1462 mol) and 300 mL of ethyl acetate. 6-Hydroxy-2-naphthaldeyde was not completely soluble even after 3 h stirring at room temperature. To this was added 3.30 g of PPTS (0.0131 mol) and the solution mixture was heated to 70° C. At this temperature, 21 g of ethyl vinyl ether (0.2912 mol) was added dropwise and the reaction mixture became homogeneous upon addition of a few drops of ethyl vinyl ether. After completion of ethyl vinyl ether addition, the reaction temperature was lowered to room temperature and the reaction mixture was stirred overnight. The crude product was purified by column chromatography (silica gel, CH2Cl2) to yield 26 g of pure 6-(1-ethoxy ethoxy)-2-naphthaldehyde (yield: 73%).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07592125B2
出典データセットuspto-grants-2009_09
ORD IDord-d081de253417462eb0dd24569da1e53f
出典メモuspto-grants-2009_09