HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 53044Generated: October 27, 2026
Ethyl Acetate → HCID 178441743, compound
https://huagongshe.com/reaction/53044
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Ethyl Acetate | HCID 8857 | — |
| Reactant | Potassium bisulfate | HCID 516920 | — |
| Reactant | 2-butyl-1H-imidazole-4,5-dicarbonitrile | HCID 5260591 | — |
| Reactant | HCID 178418310 | HCID 178418310 | — |
| Solvent | Diethyl Ether | HCID 3283 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 178441743 | HCID 178441743 | — |
Reaction Steps
A solution of 10.4 g of 2-butylimidazole-4,5-dicarbonitrile (prepared as described in Preparation 1) in 150 ml of methylene chloride was added dropwise in an atmosphere of nitrogen at 10°-15° C. to 100 ml of a 2M solution of t-butylmagnesium chloride in diethyl ether, and the mixture was stirred at the same temperature for 1 hour. 200 ml of ethyl acetate and 100 ml of aqueous potassium hydrogensulfate were then added dropwise to the reaction mixture, and the mixture was stirred at room temperature for 20 minutes. At end of this time, insoluble materials were removed by filtration, and the organic layer was separated, dried over anhydrous magnesium sulfate and concentrated by evaporation under reduced pressure. The residue was purified by column chromatography through silica gel, using a 1:3 by volume mixture of ethyl acetate and hexane as the eluent, to give 7.95 g of the title compound as crystals, melting at 135°-137° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US05616599 |
|---|
| Source dataset | uspto-grants-1997_04 |
|---|
| ORD ID | ord-aa1f18992e28478093bd1ea50e0c87ae |
|---|
| Source note | uspto-grants-1997_04 |
|---|