HuagongsheHuagongshe Chemistry Print Report · For research reference only
Ethyl iodoacetate → (1-oxo-3,4-dihydro-1H-isoquinolin-2-yl)-acetic acid ethyl ester
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Ethyl iodoacetate | HCID 12183 | — |
| Reactant | Sodium hydride | HCID 24758 | — |
| Reactant | 3,4-dihydroisoquinolin-1(2H)-one | HCID 150896 | — |
| Solvent | Toluene | HCID 1140 | — |
| Product | (1-oxo-3,4-dihydro-1H-isoquinolin-2-yl)-acetic acid ethyl ester | HCID 59764846 | — |
Reaction Steps
To a solution of 3,4-dihydro-2H-isoquinolin-1-one (0.250 g, 1.70 mmol) in toluene (5 mL) was added sodium hydride (60% in mineral oil, 0.049 g, 2.04 mmol) and the resulting suspension was heated at about reflux for about 1 h. The reaction mixture was cooled at room temperature and ethyl 2-iodoacetate (0.364 g, 1.70 mmol) was added dropwise and the mixture was again heated at about reflux for about 12 h. The reaction mixture was cooled at room temperature and filtered, rinsed with toluene. The filtrate was concentrated in vacuo to provide (1-oxo-3,4-dihydro-1H-isoquinolin-2-yl)-acetic acid ethyl ester as a peach oil (0.336 g, 1.44 mmol). The crude material was used in subsequent reactions without further purification.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08754107B2 |
| Source dataset | uspto-grants-2014_06 |
| ORD ID | ord-1d1de92b70de414f8fecb0ebfe936e74 |
| Source note | uspto-grants-2014_06 |