HuagongsheHuagongshe Chemistry Print Report · For research reference only
Iodo benzene diacetate → HCID 86673382, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Iodo benzene diacetate | HCID 12217721 | — |
| Reactant | HCID 67327185 | HCID 67327185 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 86673382 | HCID 86673382 | 98% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08722663B2 |
| Source dataset | uspto-grants-2014_05 |
| ORD ID | ord-46657cb8999a43f59f99696d15d2b1c4 |
| Source note | uspto-grants-2014_05 |