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Methanesulfonic Acid → Methanesulfonate
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|---|---|---|
| 反応物 | Methanesulfonic Acid | HCID 6395 | — |
| 反応物 | N-Methylcyclohexylamine | HCID 7514 | — |
| 反応物 | 2-(2-Ethoxy-2-phenyl-ethenyl)-1-pyrroline tetrafluoroborate | HCID 86736214 | — |
| 生成物 | Methanesulfonate | HCID 85257 | — |
| 生成物 | 2-[2-(N-methyl-cyclohexylamino)-phenylethenyl]-1-pyrroline- | HCID 53716585 | — |
反応手順
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°.
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 特許番号 | US04130652 |
| 出典データセット | uspto-grants-1978_12 |
| ORD ID | ord-e6a628c77d5e4abbaff5f78e9eabc531 |
| 出典メモ | uspto-grants-1978_12 |