HuagongsheHuagongshe Chemistry Print Report · For research reference only
Triethylamine → 4-(Chloromethyl)-6-methoxy-quinoline
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | Methanesulfonyl chloride | HCID 31297 | — |
| Reactant | 4-Hydroxymethyl-6-methoxyquinoline | HCID 338500 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | 4-(Chloromethyl)-6-methoxy-quinoline | HCID 17900617 | — |
Reaction Steps
1.16 ml of triethylamine and 0.64 ml of methanesulfonyl chloride are successively added to a solution of 1.2 g of 4-hydroxymethyl-6-methoxyquinoline in 45 ml of dichloromethane, under an inert atmosphere of argon at a temperature in the region of 20° C. Stirring is maintained at this temperature for 3 hours. The reaction medium is concentrated under reduced pressure to give a brown residue. The product is used without further purification in the following step.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07354933B2 |
| Source dataset | uspto-grants-2008_04 |
| ORD ID | ord-a487fe5f261f4611a7f4ef14eca8da73 |
| Source note | uspto-grants-2008_04 |