돌아가기
Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 629514생성일: 2026년 10월 27일

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

https://huagongshe.com/reaction/629514

반응식

참여 물질

역할이름HCID투입량
반응물DimethylamineHCID 674—
반응물DiisopropylethylamineHCID 81531—
반응물PMID26882240-Compound-8HCID 625381—
반응물1,3-Propanediamine, N'-(ethylcarbonimidoyl)-N,N-dimethyl-, monohydrochlorideHCID 2723939—
반응물1-Hydroxybenzotriazole hydrateHCID 2796029—
용매DimethylformamideHCID 6228—
용매Ethyl AcetateHCID 8857—
생성물2-(4-(adamantan-1-yl)phenoxy)-N,N-dimethylacetamideHCID 7154201091.6%

반응 단계

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).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US09315507B2
출처 데이터셋uspto-grants-2016_04
ORD IDord-6fca86eeea9946a592fceecfd07c7e06
출처 메모uspto-grants-2016_04