HuagongsheHuagongshe Chemistry Print Report · For research reference only
Tributylstannane → 6-(Benzyloxy)-3,3-dimethyl-2,3-dihydrobenzofuran
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Tributylstannane | HCID 5948 | — |
| Reactant | Benzoyl Peroxide | HCID 7187 | — |
| Reactant | 4-(Benzyloxy)-1-bromo-2-(2-methylallyloxy)benzene | HCID 66642620 | — |
| Solvent | Benzene | HCID 241 | — |
| Product | 6-(Benzyloxy)-3,3-dimethyl-2,3-dihydrobenzofuran | HCID 66642617 | 91% |
Reaction Conditions
| Temperature | 100 °C |
|---|
Reaction Steps
To a solution of 4-(benzyloxy)-1-bromo-2-(2-methylallyloxy)benzene (5.00 g, 15.1 mmol) in benzene (400 mL) was added tributyltin hydride (7.42 mL, 27.2 mmol) and benzoyl peroxide (0.70 g, 2.90 mmol) at 0° C. The resulting mixture was refluxed at 100° C. overnight. After cooling down to ambient temperature, the mixture was washed with water, dried over anhydrous sodium sulfate and filtered. The filtrate was concentrated in vacuo to dryness. The residue was subjected to column chromatography (ethyl acetate/hexane, 1/20) to give the title compound (3.48 g, 91%): MS (ES+) m/z 255.6 (M+1).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08466188B2 |
| Source dataset | uspto-grants-2013_06 |
| ORD ID | ord-bc93422e8ffa407e9657f627bfb19065 |
| Source note | uspto-grants-2013_06 |