HuagongsheHuagongshe Chemistry Print Report · For research reference only
Boron tribromide → 3-tert-butyl-6-hydroxy-2-methyl-4-phenylisoquinolin-1(2H)-one
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Boron tribromide | HCID 25134 | — |
| Reactant | 3-tert-butyl-6-methoxy-2-methyl-4-phenylisoquinolin-1(2H)-one | HCID 68509193 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | 3-tert-butyl-6-hydroxy-2-methyl-4-phenylisoquinolin-1(2H)-one | HCID 11278230 | — |
Reaction Steps
To a methylene chloride (5 mL) solution of 3-tert-butyl-6-methoxy-2-methyl-4-phenylisoquinolin-1(2H)-one (100 mg, 0.311 mmol) under argon at −70 C was added boron tribromide (1.0M, 0.934 mL, 0.934 mmol). The contents of the reaction flask were warmed to room temperature and stirred 24 h. Extracted with methylene chloride (3×), then the combined organic extracts were washed with brine and dried with anhydrous sodium sulfate. Filtration followed by evaporation of solvent in vacuo gave a solid which was triturated with ethanol. Recrystallization from ethyl acetate/ethanol afforded the title compound.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08338449B2 |
| Source dataset | uspto-grants-2012_12 |
| ORD ID | ord-ae2339bbfa844f64909d2dddfcc2ed2f |
| Source note | uspto-grants-2012_12 |