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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1627649Generated: October 25, 2026

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

https://huagongshe.com/reaction/1627649

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 numberUS08785643B2
Source datasetuspto-grants-2014_07
ORD IDord-c4f1a672dcdc44aaa480e1d67a94532e
Source noteuspto-grants-2014_07