HuagongsheHuagongshe Chemistry Print Report · For research reference only
Water → 5-[2-(p-[Ethoxycarbonylmethoxy]phenyl)ethen-1-yl]imidazo[1,5-a]pyridine
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Water | HCID 962 | — |
| Reactant | Ethyl bromoacetate | HCID 7748 | — |
| Reactant | Sodium hydride | HCID 24758 | — |
| Reactant | 5-[2-(p-Hydroxyphenyl)ethen-1-yl]imidazo[1,5-a]pyridine | HCID 54058527 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | 5-[2-(p-[Ethoxycarbonylmethoxy]phenyl)ethen-1-yl]imidazo[1,5-a]pyridine | HCID 53874958 | — |
Reaction Steps
A solution of 5-[2-(p-hydroxyphenyl)ethen-1-yl]imidazo[1,5-a]pyridine (2.36 g) in 10 ml of dimethylformamide is added to a slurry of 0.5 g of sodium hydride in 30 ml of dry dimethylformamide at 0° under nitrogen. After warming to room temperature ethyl bromoacetate (1.67 g) is added and the reaction is heated to 60° for 5 hours. Water (200 ml) is added and the solution is extracted with ethyl acetate. The combined organic phases are washed with water, dried over sodium sulfate and evaporated to yield 5-[2-(p-[ethoxycarbonylmethoxy]phenyl)ethen-1-yl]imidazo[1,5-a]pyridine.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04588732 |
| Source dataset | uspto-grants-1986_05 |
| ORD ID | ord-c6101cfb69cd4263aba46af87fd668f3 |
| Source note | uspto-grants-1986_05 |