HuagongsheHuagongshe Chemistry Print Report · For research reference only
2-Acetylbutyrolactone → 3-[1-(3-Iodoanilino)ethylidene]tetrahydro-2-furanone
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 2-Acetylbutyrolactone | HCID 10601 | — |
| Reactant | 3-Iodoaniline | HCID 12271 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | 3-[1-(3-Iodoanilino)ethylidene]tetrahydro-2-furanone | HCID 69583537 | 99.6% |
Reaction Steps
A solution of 3-iodoaniline (5.0 g, 23 mmol), α-acetyl-γ-butyrolactone (14.6 g, 0.11 mol) in ethanol (100 mL) was heated under reflux for seven days. The mixture was evaporated, and the residue was purified by silica gel column chromatography (10% ethyl acetate/hexane), to give the title compound (7.54 g) as white crystals.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06995163B2 |
| Source dataset | uspto-grants-2006_02 |
| ORD ID | ord-1dc069704bc74b65afd80a761e85316b |
| Source note | uspto-grants-2006_02 |