HuagongsheHuagongshe Chemistry Print Report · For research reference only
Triethanolamine → HCID 178473475, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Triethanolamine | HCID 7618 | — |
| Reactant | HCID 19761240 | HCID 19761240 | — |
| Reactant | HCID 131717923 | HCID 131717923 | — |
| Solvent | Toluene | HCID 1140 | — |
| Product | HCID 178473475 | HCID 178473475 | — |
Reaction Steps
4 g of the compound obtained in Stage H, 2.24 g of the compound obtained in Stage B of Example 6 and 1.7 ml of triethanolamine are refluxed in 40 ml of toluene for 24 hours. The reaction mixture is concentrated, taken up in ethyl acetate, washed with water and then extracted with 1 N hydrochloric acid, and the extract is rendered basic with concentrated sodium hydroxide solution and extracted with methylene chloride. The extract is dried to yield ethyl N-{1-[(3,4-methylenedioxybenzocyclobuten-1-yl)-methyl]-piperid-4-yl)-N-methylcarbamate. 23.5 ml of a 2% solution of fumaric acid in ethanol are added to yield the desired salt.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05214055 |
| Source dataset | uspto-grants-1993_05 |
| ORD ID | ord-2860f9933dfa489fa051731091be82e3 |
| Source note | uspto-grants-1993_05 |