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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2201455Generated: October 26, 2026

Aluminum(III) Chloride → 4-(6-Hydroxyquinazolin-2-yl)benzoic acid

https://huagongshe.com/reaction/2201455

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAluminum(III) ChlorideHCID 6451240—
Reactant4-(6-Methoxyquinazolin-2-yl)benzoic acidHCID 67974201—
SolventDichloromethaneHCID 6344—
Product4-(6-Hydroxyquinazolin-2-yl)benzoic acidHCID 5740715713%

Reaction Steps

To a suspension of 4-(6-methoxyquinazolin-2-yl)benzoic acid (220 mg, 0.785 mmol) in anhydrous CH2Cl2 (5 mL) was added AlCl3 (600 mg, 4.55 mmol), the reaction mixture was refluxed overnight. The mixture was quenched with sat. NH4Cl (10 mL), the aqueous layer was extracted with CH2Cl2/MeOH (v/v=10/1, 30 mL×3), the combined organic layer was washed with brine (30 mL), dried over Na2SO4, filtered and concentrated to give the crude product, which purified by prep-HPLC (0.1% TFA as additive) to give Compound V-1 (27 mg, yield 13%). 1H NMR (MeOD 400 MHz): δ 9.42 (s, 1H), 8.60 (d, J=8.4 Hz, 2H), 8.17 (d, J=8.4 Hz, 2H), 8.00 (d, J=9.2 Hz, 1H), 7.60 (dd, J=9.2, 2.8 Hz, 1H), 7.30 (d, J=2.8 Hz, 1H). MS (ESI): m/z 266.9 [M+H]+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09364481B2
Source datasetuspto-grants-2016_06
ORD IDord-aa7fb243dfdd46b79f0473d810a32061
Source noteuspto-grants-2016_06