Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
2,6-Lutidine → 3-(1-Methyl-1-phenyl-ethylcarbamoyl)-benzenesulfonyl chloride
참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|---|---|---|
| 반응물 | 2,6-Lutidine | HCID 7937 | — |
| 반응물 | Cumylamine | HCID 68509 | — |
| 반응물 | Benzoyl chloride, 3-(chlorosulfonyl)- | HCID 77671 | — |
| 용매 | Dichloromethane | HCID 6344 | — |
| 용매 | Ethyl Acetate | HCID 8857 | — |
| 생성물 | 3-(1-Methyl-1-phenyl-ethylcarbamoyl)-benzenesulfonyl chloride | HCID 59733690 | 106.7% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 특허 번호 | US07868023B2 |
| 출처 데이터셋 | uspto-grants-2011_01 |
| ORD ID | ord-39481ce4dd50435f94448bfb7ac8c254 |
| 출처 메모 | uspto-grants-2011_01 |