Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
Water → 1-(3-Bromophenyl)-3-heptyl-1-methylurea
참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|---|---|---|
| 반응물 | Water | HCID 962 | — |
| 반응물 | Triethylamine | HCID 8471 | — |
| 반응물 | n-Heptyl isocyanate | HCID 138341 | — |
| 반응물 | Benzenemethanamine, 3-bromo- | HCID 457587 | — |
| 용매 | Tetrahydrofuran | HCID 8028 | — |
| 용매 | Ethyl Acetate | HCID 8857 | — |
| 생성물 | 1-(3-Bromophenyl)-3-heptyl-1-methylurea | HCID 11616837 | 77% |
반응 단계
3.2 mL (20 mmol) of heptyl isocyanate are added to a solution of 2.5 g (13 mmol) of (3-bromophenyl)methylamine (prepared according to Example 24f) in 10 mL of tetrahydrofuran in the presence of 2 mL of triethylamine. The reaction mixture is stirred for 12 hours at room temperature. The reaction is stopped by addition of 2 mL of water and extraction with ethyl acetate. The organic phases are combined and dried over sodium sulfate. The solvents are evaporated off and the residue is then purified by chromatography on a column of silica eluted with a 70/30 heptane/ethyl acetate mixture. 3.4 g (77%) of 1-(3-bromophenyl)-3-heptyl-1-methylurea are obtained in the form of a solid.
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 특허 번호 | US08383652B2 |
| 출처 데이터셋 | uspto-grants-2013_02 |
| ORD ID | ord-1fe78045841c41bd8e93be2ba27e033d |
| 출처 메모 | uspto-grants-2013_02 |