HuagongsheHuagongshe Chemistry Print Report · For research reference only
Potassium Carbonate → 1-Methylisoquinoline
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | Chlorosulfonic acid | HCID 24638 | — |
| Reactant | 2,2-dimethoxy-N-(1-phenylethyl)ethanamine | HCID 60686999 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | 1-Methylisoquinoline | HCID 15592 | — |
Reaction Steps
To cooled chlorosulfonic acid (16 ml, −10° C.) was cautiously added D7 (5 g, 0.024 mol) over a period of 2 h. Reaction was allowed to warm to ambient temperature and stirring continued for 3d. The reaction was then poured into ice-water slurry (500 ml), basified using solid potassium carbonate followed by extraction using DCM. Organic phase was separated, dried over MgSO4, filtered and concentrated under reduced pressure to leave an oil. Chromatography on silica gel eluting with ethyl acetate afforded the title compound as yellow oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08063078B2 |
| Source dataset | uspto-grants-2011_11 |
| ORD ID | ord-6f96623406504cfca62cf7790d514dfd |
| Source note | uspto-grants-2011_11 |