HuagongsheHuagongshe Chemistry Print Report · For research reference only
Sodium borohydride → HCID 118114009, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Sodium borohydride | HCID 4311764 | — |
| Reactant | HCID 12439091 | HCID 12439091 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | HCID 118114009 | HCID 118114009 | 85% |
Reaction Steps
To a stirred 0° C. solution of 3-methoxy-6,7-dihydroisoquinolin-8(5H)-one (1.90 g, 10.72 mmol) in methanol (30 mL) was added sodium borohydride (1.10 g, 29.08 mmol) in small portions. The resulting mixture was allowed to warm to room temperature. After 2 h, the mixture was quenched with water (20 mL) and was extracted with ethyl acetate (3×100 mL). The combined organic phases were dried over sodium sulfate, filtered, and concentrated. Chromatographic purification of the residue (silica gel, 50% ethyl acetate in petroleum ether elute) afforded 1.60 g (85%) of 3-methoxy-5,6,7,8-tetrahydroisoquinolin-8-ol as a light yellow solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US09174986B2 |
| Source dataset | uspto-grants-2015_11 |
| ORD ID | ord-c3d8cb53ca804a31b8fc10b66a161cc2 |
| Source note | uspto-grants-2015_11 |