HuagongsheHuagongshe Chemistry Print Report · For research reference only
Boron tribromide → 1,4-Benzodioxin-6-ol, 2,3-dihydro-5-(1-methylethyl)-
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Boron tribromide | HCID 25134 | — |
| Reactant | HCID 59598692 | HCID 59598692 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | 1,4-Benzodioxin-6-ol, 2,3-dihydro-5-(1-methylethyl)- | HCID 45122030 | 65.4% |
Reaction Steps
To a solution of 5-isopropyl-6-methoxy-2,3-dihydro-benzo[1,4]dioxine (1.011 g, 4.9 mmol) in 15 ml CH2Cl2 at −78° C. was added BBr3 (7.3 ml, 7.3 mmol). The solution was allowed to warm to room temperature. After 16 hours the solution was cooled to −78° C., quenched with H2O, warmed to room temperature and extracted with CH2Cl2. The combined organics were washed with brine, dried over MgSO4, filtered and concentrated in vacuo. Purification via flash chromatography (7:3 hexane/ethyl acetate) afforded 5-isopropyl-6 hydroxy-2,3-dihydro-benzo[1,4]dioxine (0.622 g, 63%) as a pale yellow oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08524725B2 |
| Source dataset | uspto-grants-2013_09 |
| ORD ID | ord-c719ef862d824fcfb0172082b3c11a8c |
| Source note | uspto-grants-2013_09 |