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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2370208Generated: November 2, 2026

Ammonium Chloride → 2-Chloro-8-phenyl-5,6,7,8-tetrahydroquinazoline

https://huagongshe.com/reaction/2370208

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAmmonium ChlorideHCID 25517—
Reactant2,4-Dichloro-8-phenyl-5,6,7,8-tetrahydroquinazolineHCID 58075253—
CatalystZincHCID 23994—
SolventAcetoneHCID 180—
SolventWaterHCID 962—
Product2-Chloro-8-phenyl-5,6,7,8-tetrahydroquinazolineHCID 5807555752.4%

Reaction Conditions

Temperature90 °C

Reaction Steps

A mixture of 2,4-dichloro-8-phenyl-5,6,7,8-tetrahydroquinazoline (51.9 mg, 0.186 mmol), ammonium chloride (13.0 mg, 0.243 mmol) and zinc (130 mg, 1.988 mmol) in acetone (0.75 mL) and water (0.75 mL) was heated at 90° C. with stirring for 2 h. The reaction mixture was filtered through a short plug of diatomaceous earth (Celite®). The solvent was removed in vacuum, and the residue was partitioned between dichloromethane and water. The organic layer was separated and the aqueous layer was extracted with dichloromethane. The combined organic extracts were dried over anhydrous magnesium sulfate and filtered. The solvent was removed in vacuum and the residue was purified by column chromatography on silica gel to give 2-chloro-8-phenyl-5,6,7,8-tetrahydroquinazoline (24.1 mg, 0.097 mmol, 52.4% yield) as white solid. LC-MS (M+H)+=245.1. 1H NMR (500 MHz, CDCl3) δ ppm 8.39 (1H, s), 7.27 (2H, t, J=7.6 Hz), 7.16-7.23 (1H, m), 6.95 (2H, d, J=7.3 Hz), 4.21 (1H, t, J=6.0 Hz), 2.72-2.91 (2H, m), 2.14-2.26 (1H, m), 1.95-2.06 (1H, m), 1.81-1.93 (1H, m), 1.71-1.81 (1H, m).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08710061B2
Source datasetuspto-grants-2014_04
ORD IDord-e2665e4ae7f641a7b97d97aa9bea57d1
Source noteuspto-grants-2014_04