HuagongsheHuagongshe Chemistry Print Report · For research reference only
Dimethylamine → HCID 15766890, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Dimethylamine | HCID 674 | — |
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | HCID 67739237 | HCID 67739237 | — |
| Catalyst | Tetrabutylammonium hydrogen sulfate | HCID 94433 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 15766890 | HCID 15766890 | 15% |
Reaction Steps
A mixture of 5.8 g (20 mmol) of ethyl (E)-4-(5-chloroquinoline-8-yloxy)-2-butenoate, 20 ml of a 60% solution of dimethylamine in water and 0.34 g (1.0 mmol) of tetrabutylammonium hydrogen sulfate in 50 ml of dichloromethane, 40 ml of water and 10 ml of 2N sodium hydroxide solution was allowed to stand for two days at room temperature. The organic phase was separated off, and the aqueous phase was extracted twice using dichloromethane. After drying over magnesium sulfate, the solvent was stripped off in vacuo and the residue obtained was chromatographed on silica gel (ethyl acetate:heptane 7:3; followed by ethyl acetate). 1.0 g (15%) of the title compound was obtained as an oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05756422 |
| Source dataset | uspto-grants-1998_05 |
| ORD ID | ord-77ca2b8ca92246b6acb067ff5b3b74de |
| Source note | uspto-grants-1998_05 |