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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 14143생성일: 2026년 10월 26일

Butylamine → Methyl 3-[(butylamino)methyl]-5-methylbenzoate

https://huagongshe.com/reaction/14143

반응식

참여 물질

역할이름HCID투입량
반응물ButylamineHCID 8007—
반응물TriethylamineHCID 8471—
반응물Methanesulfonyl chlorideHCID 31297—
반응물Methyl 3-(hydroxymethyl)-5-methylbenzoateHCID 21086184—
용매DichloromethaneHCID 6344—
생성물Methyl 3-[(butylamino)methyl]-5-methylbenzoateHCID 21086163—

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. Butylamine (0.543 mL, 5.5 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, 89:10:1 chloroform/methanol/ammonium hydroxide) provides the title compound. 1H NMR (300 MHz, CDCl3) δ 7.75 (s, 1H), 7.70 (s, 1H), 7.24 (br s, 1H), 4.42 (d, J=9 Hz, 2H), 3.90 (s, 3H), 3.16 (m, 2H), 2.38 (s, 3H), 1.64 (s, 2H), 1.44 (m, 9H), 1.27 (m, 2H), 0.89 (t, J=7 Hz, 3H).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07727997B2
출처 데이터셋uspto-grants-2010_06
ORD IDord-da889acc1e3b408ab042d971a49859b8
출처 메모uspto-grants-2010_06