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HRID 640939作成日:2026年10月24日

Ethylene Oxide → 1-Diethylamino-3-(4-nitro-phenoxy)-propan-2-ol

https://huagongshe.com/ja/reaction/640939

反応式

関与物質

役割名称HCID仕込み量
反応物Ethylene OxideHCID 6354—
反応物DiethylamineHCID 8021—
反応物2-((4-Nitrophenoxy)methyl)oxiraneHCID 21327—
溶媒EthanolHCID 702—
生成物1-Diethylamino-3-(4-nitro-phenoxy)-propan-2-olHCID 1507248789%

反応手順

A solution of 2-(4-nitro-phenoxymethyl)-oxirane (9.75 g, 50 mmol) in absolute EtOH (100 mL) was heated at 70° C. until 2-(4-nitro-phenoxymethyl)-oxirane is dissolved then the solution was allowed to cool to room temperature. Subsequently the room temperature solution was treated with diethylamine (5.2 mL, 1.0 equiv.) in one portion. The reaction mixture is stirred at room temperature for 15 min during which time starting material (oxirane) began to precipitate out of solution. The reaction mixture was heated to 50° C. and an additional amount of diethylamine (2.6 mL) was added to achieve complete dissolution of starting oxirane. The reaction mixture was heated for an additional 5 h at 55° C. at which point thin layer chromatography (9:1, chloroform: methanol) indicated complete consumption of the starting oxirane. The reaction mixture was cooled to room temperature and concentrated in vacuo. The oily light brown residue obtained after evaporation, was purified by flash silica gel chromatography, (CHCl3 to 1:9, MeOH:CHCl3 gradient eluant) to give the 1-diethylamino-3-(4-nitro-phenoxy)-propan-2-ol as a yellow oil (11.9 g, 89%).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07692005B2
出典データセットuspto-grants-2010_04
ORD IDord-985ad3c7462549748d6aac79e615bd54
出典メモuspto-grants-2010_04