Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 507991생성일: 2026년 10월 26일
Dimethylformamide → methyl 4-[(2-methyl-3,4-dihydroquinolin-1(2H)-yl)methyl]-3-[(methylsulfonyl)oxy]benzoate
https://huagongshe.com/reaction/507991
참여 물질
| 역할 | 이름 | HCID | 투입량 |
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| 반응물 | Dimethylformamide | HCID 6228 | — |
| 반응물 | Potassium Carbonate | HCID 11430 | — |
| 반응물 | 2-Methyl-1,2,3,4-tetrahydroquinoline | HCID 96289 | — |
| 반응물 | Methyl 4-(bromomethyl)-3-[(methylsulfonyl)oxy]benzoate | HCID 23157330 | — |
| 용매 | Ethyl Acetate | HCID 8857 | — |
| 생성물 | methyl 4-[(2-methyl-3,4-dihydroquinolin-1(2H)-yl)methyl]-3-[(methylsulfonyl)oxy]benzoate | HCID 23157488 | 75% |
반응 단계
A mixture of methyl 4-(bromomethyl)-3-[(methylsulfonyl)oxy]benzoate (0.70 g, 2.2 mmol), 2-methyl-1,2,3,4-tetrahydroquinoline (0.39 g, 2.6 mmol), potassium carbonate (0.60 g, 4.3 mmol) and N,N-dimethylformamide (14 mL) was stirred at 70° C. for 23 hr. The reaction mixture was diluted with ethyl acetate, washed with water and saturated brine, dried over anhydrous magnesium sulfate, and concentrated under reduced pressure. The residue was purified by silica gel column chromatography (hexane/ethyl acetate=10/1-2/1) to give the title compound (0.63 g, yield 75%) as a pale-yellow oil.
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US07786165B2 |
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| 출처 데이터셋 | uspto-grants-2010_08 |
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| ORD ID | ord-6312856ef23848778fe07efbc22e69ae |
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| 출처 메모 | uspto-grants-2010_08 |
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