돌아가기
Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 230123생성일: 2026년 10월 25일

Dimethylformamide → 2-(4-formylphenoxy)-N-methylacetamide

https://huagongshe.com/reaction/230123

반응식

참여 물질

역할이름HCID투입량
반응물DimethylformamideHCID 6228—
반응물Oxalyl chlorideHCID 65578—
반응물Acetic acid, 2-(4-formylphenoxy)-HCID 89177—
용매DichloromethaneHCID 6344—
생성물2-(4-formylphenoxy)-N-methylacetamideHCID 15270519—

반응 단계

2-(4-formylphenoxy)acetic acid was suspended in 20 mL of DCM at 0° C., and 0.5 mL of DMF was added followed by the dropwise addition of oxalyl chloride. The solution was allowed to warm to room temperature with stirring until gas evolution stopped and the solution was homogeneous. The solution containing the crude acid chloride was concentrated under vacuum and the residue resuspended in DCM, cooled to 0° C., and methylamine and DIEA were added. The mixture was allowed to warm to room temperature with stirring over 12 hours. The reaction mixture was then poured into 5% HCl, washed 3 times with EtOAc, dried over sodium sulfate, filtered and concentrated to a thick brown oil which was purified by column using DMC/MeOH to afford 2-(4-formylphenoxy)-N-methylacetamide (9) as an off white solid. NMR (CDCl3, 400 mHz), d═9.9 (1H, s), 7.88 (2H, d, J=8.6 Hz), 7.04 (2H, d, J=8.6 Hz), 6.6-6.5 (1H, BS, 4.54 (2H, s), 2.93 (3H, d, J=4.7 Hz).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07566716B2
출처 데이터셋uspto-grants-2009_07
ORD IDord-42d66c4839a14e6cbde5bd17cf1f9a11
출처 메모uspto-grants-2009_07