HuagongsheHuagongshe Chemistry Print Report · For research reference only
Boron tribromide → 2-(4-Chloroquinazolin-2-yl)phenol
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Boron tribromide | HCID 25134 | — |
| Reactant | 4-Chloro-2-(2-methoxyphenyl)quinazoline | HCID 18071641 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | 2-(4-Chloroquinazolin-2-yl)phenol | HCID 4050956 | — |
Reaction Steps
A solution of 4-chloro-2-(2-methoxyphenyl)quinazoline (0.106 g, 0.396 mmol) in dichloromethane (4.0 mL) was treated with 1 M boron tribromide in dichloromethane (4.0 mL, 3.960 mmol) at room temperature. After 18 hours, the reaction was quenched by pouring onto ice/water (100 mL) and the aqueous phase was extracted with ethyl acetate (3×100 mL). The combined organic extracts were dried (MgSO4) and the filtrate was concentrated in vacuo. The residue was used without further purification.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08324226B2 |
| Source dataset | uspto-grants-2012_12 |
| ORD ID | ord-10471a04ff994b079a627d162d80c792 |
| Source note | uspto-grants-2012_12 |