HuagongsheHuagongshe Chemistry Print Report · For research reference only
Isoxepac → 2-(6,11-Dihydrodibenz[b,e]oxepin-2-yl)ethanol
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Isoxepac | HCID 41448 | — |
| Reactant | Borane;tetrahydrofuran | HCID 2723981 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 2-(6,11-Dihydrodibenz[b,e]oxepin-2-yl)ethanol | HCID 10728748 | 15.6% |
Reaction Steps
A solution of 6,11-dihydro-11-oxodibenz[b,e]oxepin-2-acetic acid (100 g) in 450 ml dry tetrahydrofuran (THF) at -5° C. was treated with a 1M solution of borane-THF complex (373 ml in THF) under a nitrogen blanket. After stirring at ambient temperature for 72 hours, the reaction was quenched with methanol then diluted with water. Evaporation of the organic phase left an oily biphase which was basified with saturated sodium bicarbonate and extracted into dichloromethane. The organic phase was dried and evaporated to an oil which was purified by flash chromatography to give 14 g of 2-(6,11-dihydrodibenz[b,e]oxepin-2-yl)ethanol as an oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05917057 |
| Source dataset | uspto-grants-1999_06 |
| ORD ID | ord-da485effc2a34210b4fc7bae25980eff |
| Source note | uspto-grants-1999_06 |