HuagongsheHuagongshe Chemistry Print Report · For research reference only
Water → 7-Methoxy-1,1-dimethyl-3,4-dihydronaphthalen-2(1H)-one
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Water | HCID 962 | — |
| Reactant | Methyl iodide | HCID 6328 | — |
| Reactant | Tetrahydrofuran | HCID 8028 | — |
| Reactant | 7-Methoxy-2-tetralone | HCID 77785 | — |
| Reactant | Sodium t-butoxide | HCID 23676156 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | 7-Methoxy-1,1-dimethyl-3,4-dihydronaphthalen-2(1H)-one | HCID 13011007 | — |
Reaction Steps
A slurry of sodium tert butoxide (21.1 g, 220 mmol) in THF (100 mL) was cooled to 0° C. A solution of 7-methoxy-3,4-dihydro-1H-napthalen-2-one (17.6 g, 100 mmol) and methyl iodide (30.1 g, 220 mmol) in THF (100 mL) was added dropwise over 40 min, and the reaction mixture was warmed to room temperature after 10 min. Water (200 mL) and EtOAc (600 mL) was added. The layers were separated, the organic layer was washed with water (5×100 mL) and saturated NaCl (100 mL), filtered and dried with Na2SO4 to provide the title compound (20 g).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08497287B2 |
| Source dataset | uspto-grants-2013_07 |
| ORD ID | ord-58a875f1d31c4813bbc4278c01c17a5a |
| Source note | uspto-grants-2013_07 |