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HRID 734165作成日:2026年10月26日

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

https://huagongshe.com/reaction/734165

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6-Hydroxy-2-naphthaldehydeHCID 2764110—
反応物6-Ethenylnaphthalen-2-olHCID 23135758—
生成物6-(1-Ethoxy ethoxy)-2-naphthaldehydeHCID 23135759—

反応手順

The synthesis of 6-hydroxy-2-vinylnaphthalene (HVN) was carried out by three step reactions starting from 6-hydroxy-2-naphthaldehyde. In the first step, 6-hydroxy-2-naphthaldeyde (HNAL) was protected with ethyl vinyl ether to give 6-(1-ethoxy ethoxy)-2-naphthaldehyde (EENAL). This was followed by the Wittig reaction of EENAL to yield 6-(1-ethoxy ethoxy)-2-vinylnaphthalene. Finally, this was deprotected using pyridinium p-toluenesulfonate to yield 6-hydroxy-2-vinylnaphthalene (HVN).

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-44e49d36b8344373abadf1d19721e492
出典メモuspto-grants-2009_09