HuagongsheHuagongshe Chemistry Print Report · For research reference only
Water → 6-Fluoro-7-hydroxy-3,4-dihydroisoquinolin-1(2H)-one
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Water | HCID 962 | — |
| Reactant | Ethyl Acetate | HCID 8857 | — |
| Reactant | Boron tribromide | HCID 25134 | — |
| Reactant | 6-fluoro-7-methoxy-3,4-dihydroisoquinolin-1(2H)-one | HCID 86723685 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | 6-Fluoro-7-hydroxy-3,4-dihydroisoquinolin-1(2H)-one | HCID 57567666 | 89.5% |
Reaction Steps
To a 0° C. solution of 6-fluoro-7-methoxy-3,4-dihydroisoquinolin-1(2H)-one (Cpd M, 0.428 g, 2.19 mmol) in DCM (15 mL) was added boron tribromide (1.0M in DCM, 6.00 mL, 6.00 mmol). The reaction mixture was stirred for 1 hour, then the reaction mixture was allowed to warm to room temperature. After stirring for 4 hours, water (25 mL) and EtOAc (100 mL) were added and the mixture was stirred vigorously. The layers were separated, and the organic layer was filtered and concentrated under vacuum to give 6-fluoro-7-hydroxy-3,4-dihydroisoquinolin-1(2H)-one (Cpd N, 355 mg, 89%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US09040515B2 |
| Source dataset | uspto-grants-2015_05 |
| ORD ID | ord-795a15b2a98f47dbae2a664056b1beb2 |
| Source note | uspto-grants-2015_05 |