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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 9953생성일: 2026년 10월 23일

Triethylamine → Methyl-3-[(cyclopropylcarbonylamino)methyl]-2-(methoxycarbonyl)benzoate

https://huagongshe.com/ko/reaction/9953

반응식

참여 물질

역할이름HCID투입량
반응물TriethylamineHCID 8471—
반응물Cyclopropanecarbonyl chlorideHCID 77637—
반응물Methyl-3-aminomethyl-2-(methoxycarbonyl)benzoate hydrochlorideHCID 21988538—
용매DichloromethaneHCID 6344—
생성물Methyl-3-[(cyclopropylcarbonylamino)methyl]-2-(methoxycarbonyl)benzoateHCID 21988553103%

반응 조건

온도4 °C

반응 단계

Triethylamine (1.87 g, 18 mmol) was added dropwise to a stirred suspension of methyl-3-(aminomethyl)-2-(methoxycarbonyl)benzoate hydrochloride (2.0 g, 7 mmol) in dichloromethane (40 ml). The mixture was cooled in an ice bath to 4° C. Cyclopropylcarbonyl chloride (0.99 g, 9 mmol) was added slowly at 4–8° C. After addition, the mixture was stirred in ice bath for 30 min and then warmed to room temperature for 2 hours. The mixture was washed with water (2×30 ml), brine (30 ml) and dried. Solvent was removed in vacuo and the product was purified by flash chromatography (dichloromethane/ethyl acetate 9 to 1) to give 2.1 g (93%) of the product as a white solid: 1H NMR (CDCl3) (7.87 (d, J=7.8 Hz, 1H), 7.63 (d, J=7.7 Hz, 1H), 7.46 (t, J=7.77 Hz, 1H), 6.31 (m, 1H), 4.43 (d, J=6.0 Hz, 2H), 3.95 (s, 3H), 3.90 (s, 3H), 1.36–1.29 (m, 1H), 0.99–0.93 (m, 2H), 0.76–0.69 (m, 2H).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07091353B2
출처 데이터셋uspto-grants-2006_08
ORD IDord-f680c87b1bd94a1fb587e8c844f25a45
출처 메모uspto-grants-2006_08