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HRID 1757511作成日:2026年10月24日

Chloride → 1-Phenyl-3-[3-(4-(dimethylamino)benzyloxy)phenyl]-2-propyne-1-one

https://huagongshe.com/ja/reaction/1757511

反応式

関与物質

役割名称HCID仕込み量
反応物ChlorideHCID 312—
反応物Oxalyl chlorideHCID 65578—
反応物1,3-Diphenyl-2-propyn-1-oneHCID 97637—
反応物1,3-Diphenyl-2-propyn-1-olHCID 296659—
反応物Cornforth reagentHCID 2724130—
反応物Barium manganateHCID 3084030—
溶媒Dimethyl SulfoxideHCID 679—
溶媒DichloromethaneHCID 6344—
溶媒TriethylamineHCID 8471—
生成物1-Phenyl-3-[3-(4-(dimethylamino)benzyloxy)phenyl]-2-propyne-1-oneHCID 19388218—

反応手順

In step b, the appropriate α-[(phenyl)ethynyl]-benzenemethanol compound of structure 6 can be oxidized to the corresponding 1-phenyl-3-phenyl-2-propyne-1-one compound of structure 5 by techniques and procedures well known and appreciated by one of ordinary skill in the art. For example, the appropriate α-[(phenyl)ethynyl]-benzenemethanol compound of structure 6 can be oxidized to the corresponding 1-phenyl-3-phenyl-2-propyne-1-one compound of structure 5 by means of either a Swern oxidation (dimethylsulfoxide, oxalyl chloride, and triethylamine), by means of pyridinium dichromate oxidation in a suitable aprotic solvent, such as methylene chloride or by means of barium manganate oxidation in a suitable aprotic solvent, such asmethylene chloride.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US05446068
出典データセットuspto-grants-1995_08
ORD IDord-33804668c08843c799ea85a43fce2d24
出典メモuspto-grants-1995_08