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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1743521생성일: 2026년 10월 24일

Methylamine → N-methyl-8-phenyloctanamide

https://huagongshe.com/ko/reaction/1743521

반응식

참여 물질

역할이름HCID투입량
반응물MethylamineHCID 6329—
반응물Oxalyl chlorideHCID 65578—
반응물8-Phenyloctanoic acidHCID 520273—
용매Diethyl EtherHCID 3283—
용매DichloromethaneHCID 6344—
생성물N-methyl-8-phenyloctanamideHCID 2223745583%

반응 단계

To a solution of 8-phenyl octanoic acid (28.6 g, 129.8 mmol, 1 eq) in CH2Cl2 (100 mL) cooled to 0° C. was added oxalyl chloride (17 mL, 195 mmol, 1.5 eq) dropwise via an addition funnel over 30 minutes. Upon the completion of the addition, the ice bath was removed and the reaction was stirred at rt for 2 h. It was then heated at reflux for 30 minutes. The reaction was cooled to rt and concentrated in vacuo to afford a yellow oil. It was added as a solution in Et2O (100 mL) to a solution of condensed methyl amine (˜20 mL) in Et2O (200 mL) at −78° C. Immediately, a white precipitate formed. The cold bath was removed and the reaction was allowed to stir overnight warming to rt under a stream of N2. The residue was washed with Et2O and concentrated to afford N-methyl-8-phenyloctanamide (25.2 g, 83%) as a yellow-white solid. 1H NMR (CDCl3) δ 7.68–7.10 (m, 5H); 5.42 (bs, 1H); 3.80 (m, 3H); 2.60 (m, 2H); 2.18 (m, 2H); 1.60 (m, 4H); 1.30 (m, 8H).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07008636B2
출처 데이터셋uspto-grants-2006_03
ORD IDord-4ec0cac2295c4ebcbad50bc08d884e75
출처 메모uspto-grants-2006_03