HuagongsheHuagongshe Chemistry Print Report · For research reference only
Sodium Hydroxide → 6-Hydroxy-1,2,3,4-tetrahydroisoquinolin-1-one
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | Boron tribromide | HCID 25134 | — |
| Reactant | Sodium Bicarbonate | HCID 516892 | — |
| Reactant | 6-methoxy-3,4-dihydroisoquinolin-1(2H)-one | HCID 10607392 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | 6-Hydroxy-1,2,3,4-tetrahydroisoquinolin-1-one | HCID 15908314 | — |
Reaction Steps
To a solution of 6-methoxy-1-oxo-1,2,3,4-tetrahydroisoquinoline (31.3 g, 177 mmol) in CH2Cl2 (300 mL) at -78° is added BBr3 (33.4 mL, 353 mmol). The reaction mixture is allowed to come to ambient temperature and is stirred for 12 hours. After this time the reaction mixture is cooled to 0° and is subsequently neutralized with 5N NaOH (150 mL) solution and saturated NaHCO3 solution. The resulting precipitate is extracted with hot acetone (4×500 mL) and the combined organics are concentrated in vacuo to give 6-hydroxy-1-oxo-1,2,3,4-tetrahydroisoquinoline.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05260316 |
| Source dataset | uspto-grants-1993_11 |
| ORD ID | ord-cde0f9c9426944b1bad9653365145d00 |
| Source note | uspto-grants-1993_11 |