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HRID 533495作成日:2026年10月24日

Triethanolamine → N-(9-oxo-9H-thioxanthene-2-yl)methyl-N,N,N-tris(2-hydroxyethyl)ammonium bromide

https://huagongshe.com/ja/reaction/533495

反応式

関与物質

役割名称HCID仕込み量
反応物TriethanolamineHCID 7618—
反応物2-(bromomethyl)-9H-thioxanthen-9-oneHCID 90001—
溶媒DichloromethaneHCID 6344—
生成物N-(9-oxo-9H-thioxanthene-2-yl)methyl-N,N,N-tris(2-hydroxyethyl)ammonium bromideHCID 86666340—

反応条件

温度25 °C

反応手順

The intermediate (C122-2-2) (2-bromomethylthioxanthone) (1.0 part) was dissolved in dichloromethane (85 g), and triethanol amine [product of Wako Pure Chemical industries, Ltd.] (0.5 parts) was added dropwise to this solution (an exotherm was observed after the addition). The resulting mixture was stirred at room temperature (about 25° C.) for one hour, and the organic solvent was evaporated under reduced pressure. As a result, 2.2 g of white solids were obtained. The white solids were recrystallized in a tetrahydrofuran/dichloromethane mixed solution, and 1.0 part of an intermediate (C122-2-3) was obtained (as brown solids).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08853290B2
出典データセットuspto-grants-2014_10
ORD IDord-1245c93b046441188adfc0390fd784f8
出典メモuspto-grants-2014_10