HuagongsheHuagongshe Chemistry Print Report · For research reference only
Isoquinoline → Ethyl 1-(2,4,6-trimethylphenyl)-1,2-dihydro-2-isoquinolinecarboxylate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Isoquinoline | HCID 8405 | — |
| Reactant | Ethyl chloroformate | HCID 10928 | — |
| Reactant | HCID 178425415 | HCID 178425415 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | Ethyl 1-(2,4,6-trimethylphenyl)-1,2-dihydro-2-isoquinolinecarboxylate | HCID 15895522 | — |
Reaction Steps
A solution of 2-mesitylmagnesium bromide in THP (1.0 M, 11 mL; 11 mmol) was added to an ice-cold solution of isoquinoline (1.3 g, 10 mmol) in THF (10 ml). After 5 minutes, ethyl chloroformate was added slowly dropwise and the mixture was further stirred at 0° for 10 min before quenched by saturated NH4CL solution. The mixture was poured into 0.5 N hydrochloric acid and extracted twice with ethyl ether. Combined organics were washed with brine, dried over Na2SO4, filtered, and concentrated in vacuo to give 3.58 g of titled compound (quantitative) as an oil which was used in the next reaction without further purification.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06440969B2 |
| Source dataset | uspto-grants-2002_08 |
| ORD ID | ord-67edd1157e05431b816c464a60320fa2 |
| Source note | uspto-grants-2002_08 |