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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1925317Generated: October 28, 2026

4-Chlorobenzoyl chloride → HCID 59813633, compound

https://huagongshe.com/reaction/1925317

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-Chlorobenzoyl chlorideHCID 8501—
ReactantPotassium CarbonateHCID 11430—
ReactantHCID 67520515HCID 67520515—
SolventWaterHCID 962—
SolventDichloromethaneHCID 6344—
ProductHCID 59813633HCID 59813633—

Reaction Conditions

Temperature0 °C

Reaction Steps

To a solution of 7-(6,7-dimethoxyquinolin-4-yloxy)naphthalen-2-amine (0.110 g, 0.31 mmol) in 10 ml of CH2Cl2 was added K2CO3 (0.086 g, 0.62 mmol). The mixture was cooled to 0° C. and 4-chlorobenzoyl chloride (44 mL, 0.34 mmol) was added. The solution was stirred for 16 h and allowed to gradually warm up to RT. The reaction was diluted with water and extracted with EtOAc 3×. The organic layer was dried (Na2SO4), filtered and concentrated. The residue was purified using a Gilson Prep HPLC system. The fractions were collected, combined, and extracted with EtOAc 3×. The organic layer was dried (Na2SO4), filtered and concentrated to afford the desired compound. MS (ESI, pos. ion) m/z: 485.0 (M+1). Mass Calc'd for C29H21ClN2O4: 484.937.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08178557B2
Source datasetuspto-grants-2012_05
ORD IDord-497068b3307b4568a2d8c95de1f11bd0
Source noteuspto-grants-2012_05