HuagongsheHuagongshe Chemistry Print Report · For research reference only
Ethanol → HCID 58994708, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Ethanol | HCID 702 | — |
| Reactant | HCID 67045907 | HCID 67045907 | — |
| Product | HCID 58994708 | HCID 58994708 | — |
Reaction Steps
A mixture of 3-[4-(1-bromo-butyl)-isoquinolin-1-yl]-2,4-dimethyl-phenol (110 mg, 0.29 mmol) and c-HCl (30 uL) in EtOH (12 ml) is heated at reflux for 18 h. After removal of solvent, the residue is diluted with DCM and neutralized with 1N—NaOH. The layers are separated and the aqueous layer is extracted with DCM. The combined organic layers are dried over Na2SO4 and concentrated. The residue is chromatographed on silica gel to give 19 mg of 3-[4-(1-Ethoxy-butyl)-isoquinolin-1-yl]-2,4-dimethyl-phenol along with the unreacted starting material (80 mg).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07915288B2 |
| Source dataset | uspto-grants-2011_03 |
| ORD ID | ord-d967f61211c34fa3a141e977dd1d071a |
| Source note | uspto-grants-2011_03 |