戻る
化工社化工社 化学情報印刷レポート · 研究参考用
HRID 2186658作成日:2026年10月26日

1,2-Dichloroethane → (1S,2S)-2-(3,6-dioxadecanoyl)amino-3-morpholino-1-phenyl-1-propanol

https://huagongshe.com/reaction/2186658

反応式

関与物質

役割名称HCID仕込み量
反応物1,2-DichloroethaneHCID 11—
反応物TriethylamineHCID 8471—
反応物2-(2-Butoxyethoxy)acetic acidHCID 106312—
反応物(1S,2S)-2-amino-3-morpholino-1-phenyl-1-propanolHCID 10513992—
溶媒DichloromethaneHCID 6344—
生成物(1S,2S)-2-(3,6-dioxadecanoyl)amino-3-morpholino-1-phenyl-1-propanolHCID 1204983152%

反応手順

Methylene chloride (20 ml), 3,6-dioxadecanoic acid (705.0 mg, 4.0 mmol), triethylamine (1.40 ml, 10.0 mmol) and EDC (1.15 g, 6.0 mmol) were added to (1S,2S)-2-amino-3-morpholino-1-phenyl-1-propanol (944.0 mg, 4.0 mmol), followed by stirring overnight. Methylene chloride (100 ml) was added to the reaction solution. After washed with a saturated sodium hydrogen carbonate solution (50 ml), water (50 ml) and saturated brine (50 ml) successively, the organic layer was dried over sodium sulfate and filtered, and the solvent was evaporated under reduced pressure. The resulting crude product was purified by silica gel column chromatography (chloroform:ethanol=30:1) to obtain the title compound (815 mg, yield 52%) as colorless oil.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US06407064B2
出典データセットuspto-grants-2002_06
ORD IDord-aeb1c46d5f044cbaabe65c9af7f9dd9e
出典メモuspto-grants-2002_06