HuagongsheHuagongshe Chemistry Print Report · For research reference only
Water → 3,3-Dimethyl-4-(methyloxy)-2,3-dihydro-1-benzofuran
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Water | HCID 962 | — |
| Reactant | Tributylstannane | HCID 5948 | — |
| Reactant | Azobisisobutyronitrile | HCID 6547 | — |
| Reactant | 2-Iodo-1-(methyloxy)-3-[(2-methyl-2-propen-1-yl)oxy]benzene | HCID 67966828 | — |
| Solvent | Toluene | HCID 1140 | — |
| Product | 3,3-Dimethyl-4-(methyloxy)-2,3-dihydro-1-benzofuran | HCID 57517091 | 75.8% |
Reaction Steps
To a solution of 2-iodo-1-(methyloxy)-3-[(2-methyl-2-propen-1-yl)oxy]benzene (Intermediate 4, 6.08 g) in toluene (50 ml, SCRC) were added AIBN (3.61 g, 21.99 mmol, SCRC) and tributylstannane (11.60 g, 40.0 mmol, Aldrich). The reaction mixture was heated at reflux for 3 hours and then cooled to room temperature. Water (100 ml) was added and the mixture was extracted with ethyl acetate (3 times 200 ml, SCRC). The combined organic layers were dried, evaporated and purified by silica gel chromatography with as eluents EtOAc/PE (1/50) to afford the title compound as a yellow liquid (2.7 g).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US09422272B2 |
| Source dataset | uspto-grants-2016_08 |
| ORD ID | ord-b1ea6eb1f3724b83a713c5cf7de83b7b |
| Source note | uspto-grants-2016_08 |