Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
Methanesulfonic Acid → Methanesulfonate
참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|---|---|---|
| 반응물 | Methanesulfonic Acid | HCID 6395 | — |
| 반응물 | N-Methylcyclohexylamine | HCID 7514 | — |
| 반응물 | 2-(2-Ethoxy-2-phenyl-ethenyl)-1-pyrroline tetrafluoroborate | HCID 86736214 | — |
| 생성물 | Methanesulfonate | HCID 85257 | — |
| 생성물 | 2-[2-(N-methyl-cyclohexylamino)-phenylethenyl]-1-pyrroline- | HCID 53716585 | — |
반응 단계
Crude 2-[2-(N-methylcyclohexylamino)-phenylethenyl]-1-pyrroline is produced by heating the solution of 9.1 g (0.03 mole) of 2-(2-ethoxy-2-phenyl-ethenyl)-1-pyrroline-tetrafluoroborate in 20 ml of N-methyl-cyclohexylamine for 2 hours at 100°, and processing the reaction mixture analogously to Example 1. By addition of 2.8 g of methanesulphonic acid to the solution of the crude base in isopropanol, evaporation of this solution in the rotary evaporator and recrystallisation of the residue from ethyl acetate, there is obtained 2-[2-(N-methyl-cyclohexylamino)-phenylethenyl]-1-pyrroline-(1:1)-methanesulphonate, m.p. 163°-164°.
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 특허 번호 | US04130652 |
| 출처 데이터셋 | uspto-grants-1978_12 |
| ORD ID | ord-e6a628c77d5e4abbaff5f78e9eabc531 |
| 출처 메모 | uspto-grants-1978_12 |