HuagongsheHuagongshe Chemistry Print Report · For research reference only
Sodium hydride → 5-(2-tert-Butoxycarbonylethenyl)furan-2-carboxylic acid benzyl ester
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Sodium hydride | HCID 24758 | — |
| Reactant | tert-Butyl diethylphosphonoacetate | HCID 2773685 | — |
| Reactant | 5-Formyl-2-furancarboxylic acid benzyl ester | HCID 60034788 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 5-(2-tert-Butoxycarbonylethenyl)furan-2-carboxylic acid benzyl ester | HCID 77934550 | 87.8% |
Reaction Conditions
| Temperature | 0 °C |
|---|
Reaction Steps
A solution of diethylphosphonoacetic acid tert-butyl ester (1.54 g, 6.09 mmol) in tetrahydrofuran (3 mL) was added dropwise to a suspension of 60% sodium hydride (0.19 g, 4.87 mmol) in tetrahydrofuran (50 mL) with stirring at 0° C. After stirring at room temperature for 20 minutes, a solution of 5-formyl-2-furancarboxylic acid benzyl ester (1.0 g, 4.06 mmol) in tetrahydrofuran (3 mL) was added, and the mixture was stirred at room temperature for 1 hour. The mixture was worked up according to a conventional method, and the object product was extracted by column chromatography (10-30% ethyl acetate/hexane mixed solvent) to give the title compound (1.17 g).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08877805B2 |
| Source dataset | uspto-grants-2014_11 |
| ORD ID | ord-60c85d362d064267be70c2d21bf64d16 |
| Source note | uspto-grants-2014_11 |