HuagongsheHuagongshe Chemistry Print Report · For research reference only
Diethyl Ether → HCID 178520539, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Diethyl Ether | HCID 3283 | — |
| Reactant | Ammonium Chloride | HCID 25517 | — |
| Reactant | HCID 11474387 | HCID 11474387 | — |
| Reactant | HCID 178418471 | HCID 178418471 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 178520539 | HCID 178520539 | — |
Reaction Steps
5 mmol of 4-(1-(triphenylmethyl)imidazol-4-yl)butanenitrile are introduced into a solution of 3-phenylpropylmagnesium bromide in 300 ml of diethyl ether and 100 ml of tetrahydrofuran and the mixture is brought to reflux for 6 h. Hydrolysis is carried out with an ammonium chloride solution, the organic phase is separated and the aqueous phase is stirred with dichloromethane. The combined and concentrated organic phases are brought to boiling point for 2 h in a 2N aqueous/alcohol (ethanol/water) hydrochloric acid solution. The ethanol is removed under vacuum, filtration is carried out and basification is carried out. The title compound is stirred in dichloromethane and recrystallized in the hydrogenmaleate form from ethanol/diethyl ether.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05559113 |
| Source dataset | uspto-grants-1996_09 |
| ORD ID | ord-558dad95af7248079e9209386a495763 |
| Source note | uspto-grants-1996_09 |