HuagongsheHuagongshe Chemistry Print Report · For research reference only
Boron tribromide → 2-(3-hydroxyphenyl)quinazolin-4(3H)-one
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Boron tribromide | HCID 25134 | — |
| Reactant | 2-(3-methoxyphenyl)quinazolin-4(3H)-one | HCID 135486399 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | 2-(3-hydroxyphenyl)quinazolin-4(3H)-one | HCID 135567246 | — |
Reaction Conditions
| Temperature | -78 °C |
|---|
Reaction Steps
To 2-(3-methoxyphenyl)quinazolin-4(3H)-one (11.6 g, 45.98 mmole) was added of CH2Cl2 (120 mL) and the mixture was cooled to −78° C. Then, a 1 M solution of BBr3 in CH2Cl2 (60 mL, 60.0 mmol) was added drop wise and the reaction was stirred at −78° C. for 1 h and then ambient temperature for 3 h. The reaction was re-cooled to −78° C. and cautiously quenched with MeOH (20 mL). The ice bath was removed and the system allowed to stir at ambient temperature for 0.5 h. The pH was adjusted to 7 with 10% w/w NaHCO3 solution. The solid was filtered, washed with ether, dried and then azeotroped from toluene (3 X) and dried under high vacuum overnight to give 2-(3-hydroxyphenyl)quinazolin-4(3H)-one. (11.0 g, mmol, 100%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US09440961B2 |
| Source dataset | uspto-grants-2016_09 |
| ORD ID | ord-ec8ecfd06b184fdd881c4efedc514ac4 |
| Source note | uspto-grants-2016_09 |