HuagongsheHuagongshe Chemistry Print Report · For research reference only
Tetrahydrofuran → HCID 18333022, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Tetrahydrofuran | HCID 8028 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | Methanesulfonyl chloride | HCID 31297 | — |
| Reactant | HCID 15542694 | HCID 15542694 | — |
| Solvent | Potassium Bicarbonate | HCID 516893 | — |
| Product | HCID 18333022 | HCID 18333022 | 71.1% |
Reaction Steps
Methanesulfonyl chloride (0.6 g) was added to a THF (20 ml) solution of 3-(N,N-dimethylamino)methyl-1,2,3,4-tetrahydroquinoline (Reference Example 44; 1 g) under ice-cooling. The reaction mixture was stirred at room temperature for 10 minutes, to which was added triethylamine (2 ml), and the mixture was further stirred at room temperature for 3 hours. The reaction mixture was diluted with a saturated aqueous potassium bicarbonate solution and extracted with ethyl acetate. The organic layer was washed with water, then dried and concentrated. The residue was purified by alumina column chromatography (eluent: ethyl acetate) and recrystallized from IPE to obtain the entitled compound (1 g).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06329389B1 |
| Source dataset | uspto-grants-2001_12 |
| ORD ID | ord-98a6af9b6ee44b4aa79429237031824a |
| Source note | uspto-grants-2001_12 |