HuagongsheHuagongshe Chemistry Print Report · For research reference only
Ethanesulfonic acid → HCID 19428157, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Ethanesulfonic acid | HCID 11668 | — |
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | HCID 19428170 | HCID 19428170 | — |
| Solvent | Chloroform | HCID 6212 | — |
| Solvent | Water ethanol | HCID 19096565 | — |
| Product | HCID 19428157 | HCID 19428157 | 59% |
Reaction Steps
Alternative process: 1.3 g (3.1 mmol) of 6-hydroxy-7-methoxy-3-{2-[4-(2-methoxyphenyl)-1-piperazinyl]ethyl}-4-methyl-2H-1-benzopyran-2-one (Example 2), two equivalents of sodium hydroxide and 2.5 equivalents of ethanesulphonic acid are dissolved in water/ethanol and stirred for 60 hours at room temperature. The reaction product is taken up in chloroform, washed with dilute sodium hydroxide and with water, dried over sodium sulphate, and the solvent is removed under reduced pressure. 0.94 g (59%) of pale yellow crystals with a melting point of 148°-150° C. (from ethanol/TBME) are obtained by column chromatography over silica gel (solvent: acetone/petroleum ether 1/1).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05550129 |
| Source dataset | uspto-grants-1996_08 |
| ORD ID | ord-73df0f2977324bd5b68b46cd3b76f5a2 |
| Source note | uspto-grants-1996_08 |