HuagongsheHuagongshe Chemistry Print Report · For research reference only
Thionyl Chloride → HCID 21891598, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Thionyl Chloride | HCID 24386 | — |
| Reactant | HCID 21891575 | HCID 21891575 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 21891598 | HCID 21891598 | — |
Reaction Steps
Thionyl chloride (1.7 mL) was added to a solution of 2-hydroxymethyl-5,6,7-trimethoxyquinoline (1.45 g) in dichloromethane (15 mL) under ice cooling, and the mixture was stirred at room temperature for 30 minutes. After concentrating the reaction mixture under reduced pressure, an aqueous solution of potassium carbonate was added to the residue to alkalify it. The thus-treated residue was extracted with diethyl ether. The resultant organic layer was washed with water and saturated brine, dried over anhydrous magnesium sulfate and then concentrated under reduced pressure, and the residue was purified by column chromatography on silica gel (ethyl acetate:hexane=1:2) to obtain the title compound.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07135473B2 |
| Source dataset | uspto-grants-2006_11 |
| ORD ID | ord-e4368a7d227345d9afc744270f4b5076 |
| Source note | uspto-grants-2006_11 |