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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 252228생성일: 2026년 10월 25일

2,6-Lutidine → 3-(1-Methyl-1-phenyl-ethylcarbamoyl)-benzenesulfonyl chloride

https://huagongshe.com/reaction/252228

반응식

참여 물질

역할이름HCID투입량
반응물2,6-LutidineHCID 7937—
반응물CumylamineHCID 68509—
반응물Benzoyl chloride, 3-(chlorosulfonyl)-HCID 77671—
용매DichloromethaneHCID 6344—
용매Ethyl AcetateHCID 8857—
생성물3-(1-Methyl-1-phenyl-ethylcarbamoyl)-benzenesulfonyl chlorideHCID 59733690106.7%

반응 단계

3-Chlorosulfonyl-benzoyl chloride (1 g, 4.2 mmol) was dissolved in DCM (10 mL) and cooled in an ice bath. To the solution was added 1-methyl-1-phenyl-ethylamine (0.9 g, 3.8 mmol) and 2,6-lutidine (1 mL, 8.4 mmol). The mixture was allowed to warm up to RT and stirred for 4 h. The reaction mixture was diluted with EtOAc (100 mL) and washed with 1 N HCl (2×75 mL) and brine. The organic layer was dried (MgSO4) and evaporated in vacuo to provide 1.37 g (98%) of 3-(1-methyl-1-phenyl-ethylcarbamoyl)-benzenesulfonyl chloride as a tan solid. 1H-NMR (CDCl3): δ 8.40 (t, 1H, J=1.7 Hz), 8.15-8.18 (m, 2H), 7.72 (t, 1H, J=7.8 Hz), 7.46-7.50 (m, 2H), 7.36-7.41 (m, 2H), 7.27-7.32 (m, 1H), 6.56 (br s, 1H), and 1.87 (s, 6H).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07868023B2
출처 데이터셋uspto-grants-2011_01
ORD IDord-39481ce4dd50435f94448bfb7ac8c254
출처 메모uspto-grants-2011_01