HuagongsheHuagongshe Chemistry Print Report · For research reference only
2-(2-Nitrovinyl)-5-phenylfuran → 2-Furanethanamine, 5-phenyl-
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 2-(2-Nitrovinyl)-5-phenylfuran | HCID 801279 | — |
| Reactant | Aluminium lithium hydride | HCID 21226445 | — |
| Product | 2-Furanethanamine, 5-phenyl- | HCID 24838269 | 20.3% |
Reaction Steps
Cool lithium aluminum hydride (21 mL, 1.0 M solution in ether) to 0° C. and add 2-(2-nitrovinyl)-5-phenylfuran (760 mg, 3.53 mmol in 5 mL of ether). Stir reaction to room temperature for 15 hours. Re-cool reaction to 0° C. and quench with 0.80 mL of water, followed by 0.80 mL 1M sodium hydroxide and 0.80 mL of water (×3). Dilute reaction with additional tetrahydrofuran and stir at room temperature for 2 hours. Filter and dry over sodium sulfate and filter again. Concentrate and perform flash column chromatography (methylene chloride, MeOH, NH4OH) to give 134 mg (20% yield) of the title compound as a brown oil. MH+ 188.0.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07265246B2 |
| Source dataset | uspto-grants-2007_09 |
| ORD ID | ord-978aa5b525f84227a4dcd45260e51ec9 |
| Source note | uspto-grants-2007_09 |