HuagongsheHuagongshe Chemistry Print Report · For research reference only
Benzyl Bromide → 4-Benzyloxy-1-bromo-isoquinoline-3-carboxylic acid butyl ester
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Benzyl Bromide | HCID 7498 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | 1-Bromo-4-hydroxy-isoquinoline-3-carboxylic acid butyl ester | HCID 86014541 | — |
| Solvent | Acetone | HCID 180 | — |
| Product | 4-Benzyloxy-1-bromo-isoquinoline-3-carboxylic acid butyl ester | HCID 86014503 | — |
Reaction Steps
A mixture of 1-bromo-4-hydroxy-isoquinoline-3-carboxylic acid butyl ester (6.48 g, 20 mmol; Example D-28 a), benzyl bromide (3.6 ml, 30 mmol), K2CO3 (12.44 g, 90 mmol) and acetone (300 ml) was refluxed with stirring for 2.5 d. The solvent was then evaporated in vacuo. To the residue was added water (100 ml) and the mixture was extracted with EtOAc (100 ml). The organic phase was dried over MgSO4 and evaporated in vacuo to give the title compound as a yellowish solid; MS-(+)-ion: M+1=414.1.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07863292B2 |
| Source dataset | uspto-grants-2011_01 |
| ORD ID | ord-fc8d1a74afb84d69a3ef9241881514b9 |
| Source note | uspto-grants-2011_01 |