HuagongsheHuagongshe Chemistry Print Report · For research reference only
Sodium borohydride → HCID 66606820, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Sodium borohydride | HCID 4311764 | — |
| Reactant | HCID 68746412 | HCID 68746412 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | HCID 66606820 | HCID 66606820 | 95% |
Reaction Steps
Step 2 A suspension of 2-(3-bromo-2-methylphenyl)isoquinoline-1,3(2H,4H)-dione (630 mg, 1.908 mmol) in methanol (100 mL) was treated with sodium borohydride (217 mg, 5.72 mmol) at rt. After 1.5 h, additional sodium borohydride (120 mg) was added. After 7 h, the mixture was concentrated and the residue was partitioned between water and DCM. The organic phase was dried and concentrated to give 2-(3-bromo-2-methylphenyl)-3-hydroxy-3,4-dihydroisoquinolin-1(2H)-one as a light yellow foam (600 mg, 95%), used without further purification. Mass spectrum m/z 332, 334 (M+H)+.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08084620B2 |
| Source dataset | uspto-grants-2011_12 |
| ORD ID | ord-e67c627a8b3c42afaf82a0f58ba486ca |
| Source note | uspto-grants-2011_12 |