HuagongsheHuagongshe Chemistry Print Report · For research reference only
Sodium hydride → Methyl (2E)-3-(1-methyl-1H-imidazol-4-yl)-2-propenoate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Sodium hydride | HCID 24758 | — |
| Reactant | Methyl diethylphosphonoacetate | HCID 66113 | — |
| Reactant | 1-Methyl-1H-imidazole-4-carbaldehyde | HCID 573419 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | Methyl (2E)-3-(1-methyl-1H-imidazol-4-yl)-2-propenoate | HCID 13944045 | 57.5% |
Reaction Conditions
| Temperature | 0 °C |
|---|
Reaction Steps
1 ml (5.5 mmol) of methyl diethylphosphonoacetate are added to a suspension of 220 mg (5.5 mmol) of sodium hydride at 60% in 5 ml of tetrahydrofuran cooled to 0° C. After stirring for 1 h, 500 mg (4.5 mmol) of 1-methyl-1H-imidazole-4-carbaldehyde are added and the mixture is stirred for 4 hours at ambient temperature and then hydrolysed with water and extracted with ethyl acetate. The organic phase is washed with a saturated aqueous solution of sodium hydrogen carbonate, dried over magnesium sulphate, filtered and evaporated. The product obtained is precipitated from heptane and filtered. 430 mg of methyl (E)-3-(1-methyl-1H-imidazol-4-yl)acrylate are obtained in the form of a yellow powder with a yield of 57%.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08871187B2 |
| Source dataset | uspto-grants-2014_10 |
| ORD ID | ord-5e3b943bd15746d69f4f64761bc1fcd9 |
| Source note | uspto-grants-2014_10 |