HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1406879Generated: October 30, 2026
Boron tribromide → 2-(3-hydroxyphenyl)quinazolin-4(3H)-one
https://huagongshe.com/reaction/1406879
Participants
| Role | Name | HCID | Charge |
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| 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 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×) 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 |
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| Patent number | US08916576B2 |
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| Source dataset | uspto-grants-2014_12 |
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| ORD ID | ord-d6abae01e8684fa7b87fe1d9883e107f |
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| Source note | uspto-grants-2014_12 |
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