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HRID 1885421作成日:2026年10月25日

Diethyl Ether → 3-Phenoxybenzyl 2-(3-chloro-4-hydroxyphenyl)-2-methylpropyl ether

https://huagongshe.com/reaction/1885421

反応式

関与物質

役割名称HCID仕込み量
反応物Diethyl EtherHCID 3283—
反応物Potassium HydroxideHCID 14797—
反応物3-Chloro-4-ethoxyneophyl 3-phenoxybenzyl etherHCID 3067183—
溶媒1,3-Dimethyl-2-imidazolidinoneHCID 6661—
生成物3-Phenoxybenzyl 2-(3-chloro-4-hydroxyphenyl)-2-methylpropyl etherHCID 1105807050%

反応手順

With respect to the production of the compound of the formula (II), there is known only a process disclosed in Japanese Patent Application Kokai (Laid-Open) No. 212335/1987. The document discloses a process for producing 3-chloro-4-hydroxyneophyl m-phenoxybenzyl ether [a compound of the formula (II) wherein X1 =Cl and X2 =H] by subjecting 4-ethoxy-3-chloroneophyl m-phenoxybenzyl ether to an ether cleavage reaction. It is specifically a process comprising subjecting 4-ethoxy-3-chloroneophyl m-phenoxybenzyl ether to ether cleavage in N,N'-dimethylimidazolidinone, using excessive potassium hydroxide as an ether cleavage agent. According to the document, 4-hydroxy-3-chloroneophyl m-phenoxybenzyl ether was obtained under the reaction conditions of 150° C. and 18 hours, but the yield was as low as about 50%.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US05144083
出典データセットuspto-grants-1992_09
ORD IDord-c7043777428243af95a3c81b81006f4a
出典メモuspto-grants-1992_09