HuagongsheHuagongshe Chemistry Print Report · For research reference only
Triethylamine → 4-Quinolinylmethyl methanesulfonate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | Methanesulfonyl chloride | HCID 31297 | — |
| Reactant | 4-(Hydroxymethyl)quinoline | HCID 80479 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | 4-Quinolinylmethyl methanesulfonate | HCID 13540821 | — |
Reaction Steps
A solution of methanesulfonyl chloride (4.84 ml) in 20 ml of methylene chloride is slowly added over 20 minutes to a solution of 8.29 g of 4-hydroxymethylquinoline and 11 ml of triethylamine in 200 ml of methylene chloride at 0°. After completion of the reaction at room temperature, the reaction mixture is partitioned between methylene chloride and saturated potassium carbonate solution. The organic layer is dried over sodium sulfate and evaporated to dryness to yield 4-(methanesulfonyloxymethyl)quinoline as an oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05057506 |
| Source dataset | uspto-grants-1991_10 |
| ORD ID | ord-e4e7426ef6fa41e792a4f1e4567005dd |
| Source note | uspto-grants-1991_10 |