HuagongsheHuagongshe Chemistry Print Report · For research reference only
Sodium borohydride → 58794-07-3
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Sodium borohydride | HCID 4311764 | — |
| Reactant | HCID 53403113 | HCID 53403113 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | 58794-07-3 | HCID 82575882 | — |
Reaction Steps
1-(isoquinolin-8-yl)ethanone (0.64 g, 3.74 mmol) in EtOH (37 mL) was added with sodium borohydride (2.26 g, 59.8 mmol). The reaction mixture was stirred overnight. The reaction mixture was quenched with 1M NaOH and extracted with DCM. Purified by normal phase chromatography (10-60% EtOAc in hexane) to yield 1-(isoquinolin-8-yl)ethanol as an oil. Chiral separation (ChiralPak AD-H) provided (S)-1-(isoquinolin-8-yl)ethanol and (R)-1-(isoquinolin-8-yl)ethanol.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US09273040B2 |
| Source dataset | uspto-grants-2016_03 |
| ORD ID | ord-8368ae2540fb4ea99bdb01974583b9eb |
| Source note | uspto-grants-2016_03 |