Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1686152Generated: November 1, 2026

Benzoyl chloride → HCID 86627417, compound

https://huagongshe.com/reaction/1686152

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzoyl chlorideHCID 7412—
ReactantTriethylamineHCID 8471—
ReactantHCID 86627418HCID 86627418—
SolventDichloromethaneHCID 6344—
ProductHCID 86627417HCID 86627417—

Reaction Steps

4-(2-Aminoethoxy)-2-(2-bromobenzyloxy)benzaldehyde (200 mg, 0.43 mmol) was dissolved in CH2Cl2 (20 ml) and Et3N (87.02 mg, 0.12 ml, 0.86 mmol) was added to the solution, followed by stirring for 2˜3 min. Benzoyl chloride (60.45 mg, 50 μl, 0.43 mmol) was also added before additionally stirring at room temperature for 2 hours. After completion of the reaction, the reaction solution was extracted with brine and CH2Cl2 (×3). The organic layer was dried over anhydrous MgSO4 and filtered. The filtrate was concentrated in a vacuum. The residue was purified using column chromatography (ethyl acetate/n-hexane=1/5→1/3) to afford the object compound (white solid, 78 mg, 40%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08148541B2
Source datasetuspto-grants-2012_04
ORD IDord-fe14dd9cf995435f827a2ee6df78eca7
Source noteuspto-grants-2012_04