HuagongsheHuagongshe Chemistry Print Report · For research reference only
Dichloromethane → Ethyl 1-phenyl-3,4-dihydro-1H-isoquinoline-2-carboxylate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Dichloromethane | HCID 6344 | — |
| Reactant | Ethyl chloroformate | HCID 10928 | — |
| Reactant | 1,2,3,4-Tetrahydro-1-phenylisoquinoline | HCID 100137 | — |
| Solvent | Triethylamine | HCID 8471 | — |
| Product | Ethyl 1-phenyl-3,4-dihydro-1H-isoquinoline-2-carboxylate | HCID 10423841 | — |
Reaction Steps
To a 130 ml dichloromethane solution containing 6.28 g of 1-phenyl-1,2,3,4-tetrahydroisoquinoline and 3.34 g of triethylamine, 3.1 ml of ethyl chloroformate was added dropwise under ice-cooling, followed by stirring at room temperature overnight. The reaction solution was washed successively with water, 1N hydrochloric acid, water and brine and then dried over anhydrous sodium sulfate. The solvent was removed under reduced pressure, thereby 10.58 g of ethyl 1-phenyl-1,2,3,4-tetrahydro-2-isoquinolinecarboxylate was obtained as pale yellow oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06017927 |
| Source dataset | uspto-grants-2000_01 |
| ORD ID | ord-d34a8cf1bdd142488f513847084b3196 |
| Source note | uspto-grants-2000_01 |