HuagongsheHuagongshe Chemistry Print Report · For research reference only
Diethyl Ether → Isoquinoline, 4-bromo-7-chloro-, 2-oxide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Diethyl Ether | HCID 3283 | — |
| Reactant | m-Chloroperbenzoic acid | HCID 70297 | — |
| Reactant | 4-Bromo-7-chloroisoquinoline | HCID 56973329 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | Isoquinoline, 4-bromo-7-chloro-, 2-oxide | HCID 68900861 | — |
Reaction Steps
4-bromo-7-chloroisoquinoline (3-6)(1 g, 4.12 mmol, 1.0 equiv.) was dissolved in anhydrous CH2Cl2 (8.2 mL) and treated with mCPBA (1.622 g, 9.40 mmol, 2.3 equiv.). The reaction mixture was stirred at room temperature, forming 3-7 as a white precipitate. Following dilution with Et2O, the solid was collected and used without further purification in the next step. LRMS m/z (M+H) 260.1 found, 259.9 required.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07501435B2 |
| Source dataset | uspto-grants-2009_03 |
| ORD ID | ord-efc5cfcb18e3442fbfddda25730b794d |
| Source note | uspto-grants-2009_03 |