HuagongsheHuagongshe Chemistry Print Report · For research reference only
Ethyl bromoacetate → HCID 13059431, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Ethyl bromoacetate | HCID 7748 | — |
| Reactant | Sodium hydride | HCID 24758 | — |
| Reactant | HCID 13059430 | HCID 13059430 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 13059431 | HCID 13059431 | 54% |
Reaction Steps
A solution of methyl 4-(1H-imidazol-1-yl)-β-oxobenzenepropanoate (6.1 g, 0.025 mol) in tetrahydrofuran (65 ml) is added slowly to a stirred suspension of 50% NaH (1.2 g, 0.025 mol) in tetrahydrofuran (20 ml) and the solution is stirred for one additional hour. Ethyl bromoacetate (4.5 g) is added followed by refluxing the mixture for 7 to 8 hours. The tetrahydrofuran is removed, the residue is treated with water, and the organic material is extracted with ether. The residue obtained after removal of ether is hydrolysed by heating with 6 N HCl for 7 to 8 hours. The crude acid is finally crystallized from dimethylformamide to yield 3.3 g of the product 4-(1H-imidazol-1-yl)-γ-oxobenzenebutanoic acid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04353905 |
| Source dataset | uspto-grants-1982_10 |
| ORD ID | ord-8c1af3a66af94737afaa498744771152 |
| Source note | uspto-grants-1982_10 |