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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1023344Generated: October 30, 2026

Iodo benzene diacetate → HCID 86673382, compound

https://huagongshe.com/reaction/1023344

Reaction equation

Participants

RoleNameHCIDCharge
ReactantIodo benzene diacetateHCID 12217721—
ReactantHCID 67327185HCID 67327185—
SolventDichloromethaneHCID 6344—
ProductHCID 86673382HCID 8667338298%

Reaction Steps

To a CH2Cl2 (38 mL) solution of [2-(4-methoxyphenoxy)quinolin-6-yl]methanol (1.11 g) and iodobenzene diacetate (1.33 g) was added 2,2,6,6-tetramethyl-1-piperidinyloxy radical (61.0 mg), then the resultant mixture was stirred over night at room temperature. The reaction mixture was quenched by addition of saturated aqueous Na2S2O3 and NaHCO3, and extracted with CH2Cl2. The organic layer was washed with water and saturated aqueous NaCl, dried over anhydrous Na2SO4, and concentrated under reduced pressure. The residue was purified by silica gel column chromatography (n-hexane/AcOEt=10/1 to 5/1) to afford 2-(4-methoxyphenoxy)quinoline-6-carbaldehyde (1.08 g) as a colorless solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08722663B2
Source datasetuspto-grants-2014_05
ORD IDord-46657cb8999a43f59f99696d15d2b1c4
Source noteuspto-grants-2014_05