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HRID 629514作成日:2026年10月27日

Dimethylamine → 2-(4-(adamantan-1-yl)phenoxy)-N,N-dimethylacetamide

https://huagongshe.com/reaction/629514

反応式

関与物質

役割名称HCID仕込み量
反応物DimethylamineHCID 674—
反応物DiisopropylethylamineHCID 81531—
反応物PMID26882240-Compound-8HCID 625381—
反応物1,3-Propanediamine, N'-(ethylcarbonimidoyl)-N,N-dimethyl-, monohydrochlorideHCID 2723939—
反応物1-Hydroxybenzotriazole hydrateHCID 2796029—
溶媒DimethylformamideHCID 6228—
溶媒Ethyl AcetateHCID 8857—
生成物2-(4-(adamantan-1-yl)phenoxy)-N,N-dimethylacetamideHCID 7154201091.6%

反応手順

A suspension of 2-(4-(adamantan-1-yl)phenoxy)acetic acid (0.2 g, 0.69 mmol), dimethylamine (0.031 g, 0.69 mmol), 1-ethyl-3-(3-dimethylaminopropyl)carbodiimide HCl (EDCI) (0.16 g, 0.83 mmol) and 1-hydroxybenzotriazole hydrate (HOBt) (0.11 g, 0.83 mmol) in N,N-dimethylformamide (2 mL) was added N,N-diisopropylethylamine (DIPEA) (0.106 mL, 1.74 mmol) and stirred at room temperature under nitrogen overnight. Reaction mixture was diluted with ethyl acetate and subsequentially washed with aqueous sodium hydroxide and brine. The organic layer was dried over anhydrous magnesium sulfate. The solvent was filtered and evaporated under reduced pressure to afford a crude solid, which was purified by silica gel column chromatography to give 2-(4-(adamantan-1-yl)phenoxy)-N,N-dimethylacetamide as a white solid (0.198 g, 90.3% yield).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US09315507B2
出典データセットuspto-grants-2016_04
ORD IDord-6fca86eeea9946a592fceecfd07c7e06
出典メモuspto-grants-2016_04