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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 14133생성일: 2026년 10월 25일

Triethylamine → Methyl 3-{[isobutyl(methyl)amino]methyl}-5-methylbenzoate

https://huagongshe.com/reaction/14133

반응식

참여 물질

역할이름HCID투입량
반응물TriethylamineHCID 8471—
반응물N-MethylisobutylamineHCID 12249—
반응물Methanesulfonyl chlorideHCID 31297—
반응물Methyl 3-(hydroxymethyl)-5-methylbenzoateHCID 21086184—
용매DichloromethaneHCID 6344—
생성물Methyl 3-{[isobutyl(methyl)amino]methyl}-5-methylbenzoateHCID 21086186—

반응 단계

To an ice-cold, stirred solution of methyl 3-(hydroxymethyl)-5-methylbenzoate (200 mg, 1.1 mmol) in methylene chloride (2.2 mL) is added triethylamine (0.304 mL, 2.2 mmol) followed by methanesulfonyl chloride (0.116 mL, 1.5 mmol). The reaction mixture is stirred for 15 min and filtered. N-Methylisobutylamine (287 mg, 3.3 mmol) is added to the filtrate, and the reaction mixture is stirred at room temperature for 5 h. The reaction mixture is diluted with methylene chloride (10 mL), washed with 1 N hydrochloric acid, and saturated sodium bicarbonate, dried (magnesium sulfate), filtered, and concentrated under reduced pressure. Purification by flash column chromatography (silica, 15% ethyl acetate/hexanes) provides the title compound. 1H NMR (300 MHz, CDCl3) δ 7.77 (s, 1H), 7.73 (s, 1H), 7.36 (s, 1H), 3.90 (s, 3H), 3.44 (s, 2H), 2.38 (s, 3H), 2.14 (s, 3H), 2.10 (d, J=8 Hz, 2H), 1.81 (m, 1H), 0.90 (d, J=7 Hz, 6H).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07727997B2
출처 데이터셋uspto-grants-2010_06
ORD IDord-ebeebd16d2ba4b0ab5865ad9622d68d2
출처 메모uspto-grants-2010_06