HuagongsheHuagongshe Chemistry Print Report · For research reference only
Potassium Hydroxide → (R)-(7-Bromo-2,3-dihydrobenzo[b][1,4]dioxin-2-yl)methanol
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Potassium Hydroxide | HCID 14797 | — |
| Reactant | 5-Bromo-2-[(2S)-oxiran-2-ylmethoxy]phenyl formate | HCID 86652942 | — |
| Solvent | 1,4-Dioxane | HCID 31275 | — |
| Product | (R)-(7-Bromo-2,3-dihydrobenzo[b][1,4]dioxin-2-yl)methanol | HCID 66879096 | 57.9% |
Reaction Steps
5-bromo-2-[(2S)-oxiran-2-ylmethoxy]phenyl formate (8.5 g, 31 mmol) was dissolved in dioxane. At 0° C., KOH (10%) was added. The mixture was stirred in rt for 1 h and 30 min and was then concentrated. Water was added. Aqueous HCl (1 N) was added to neutralize and the solution was then extracted with EtOAc (3×75 ml). The combined organic phases were washed with brine, dried (Na2SO4) and evaporated to dryness. Purification on flash column chromatography (isooctane/EtOAc) gave the crude title compound (4.4 g). MS m/z (rel. intensity, 70 eV) 245 (M+, 97) 244 (M+, bp), 189 (48), 188 (50) 70 (39).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08524766B2 |
| Source dataset | uspto-grants-2013_09 |
| ORD ID | ord-61f24cfec60f48afa1900c5526d9dd01 |
| Source note | uspto-grants-2013_09 |