Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Hexane | HCID 8058 | — |
| Reactant | 3,5-Dimethoxybenzaldehyde | HCID 81747 | — |
| Reactant | 7-bromo-3,4-dihydro-2H-1,5-benzodioxepine | HCID 2776394 | — |
| Reactant | Butyllithium | HCID 178418339 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Isopropanol | HCID 3776 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 69203973 | HCID 69203973 | 95% |
Reaction Steps
To a solution of 7-bromo-3,4-dihydro-2H-benzo[b][1,4]dioxepine (1.7 g, 7.4 mmol) in THF (10 mL) was added a solution of n-butyllitium in hexane (2.6 mL, 2.5 N, 6.5 mmol) at −78° C. and kept for 20 min. To the mixture was added a solution of 3,5-dimethoxy-benzaldehyde (1.0 g, 6.0 mmol) in THF (10 mL) at −78° C. After 2 h, isopropanol (2 mL) and water (10 mL) was added to the mixture, and the cold bath was removed. The mixture was stirred at room temperature for 20 min. The mixture was extracted with ethyl acetate (50 mL) and water (50 mL). The aqueous layer was extracted with ethyl acetate (50 mL). The combined organic layers was washed with HCl (1N, 50 mL), water (50 mL), brine (50 mL) and dried over MgSO4. Removal of solvent and chromatography (Silica Gel) gave (3,4-dihydro-2H-benzo[b][1,4]dioxepin-7-yl)-(3,5-dimethoxy-phenyl) -methanol as an oil (1.8 g, 95% yield): 1H NMR (CDCl3) δ 2.16-2.22 (m, 2H, CH2), 3.77 (s, 6H, 2CH3), 4.16-4.21 (m, 4H, 2CH2), 5.67 (d, J=3 Hz, 1H, CH), 6.35 (t, J=2 Hz, 1H, Ar), 6.54 (d, J=2 Hz, 1H, Ar), 6.92 (d, J=1 Hz, 2H, Ar), 6.98 (s, 1H, Ar).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US07470723B2 |
|---|
| Source dataset | uspto-grants-2008_12 |
|---|
| ORD ID | ord-848b6754f118489898ada89e610b9894 |
|---|
| Source note | uspto-grants-2008_12 |
|---|