HuagongsheHuagongshe Chemistry Print Report · For research reference only
3-Quinolinecarboxaldehyde → (Quinolin-3-yl)methanol
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 3-Quinolinecarboxaldehyde | HCID 83641 | — |
| Reactant | Sodium borohydride | HCID 4311764 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | (Quinolin-3-yl)methanol | HCID 12662983 | 86% |
Reaction Steps
Sodium borohydride (240 mg, 6.4 mmol) was added in portions to a solution of 3-Quinoline-carboxaldehyde (910 mg, 5.8 mmol) in methanol at room temperature. Reaction was quenched after 3 hours stirring with 10 mls (aq) sat. NH4Cl. Mixture was extracted with ethyl acetate (3×30 ml). Combined organics were washed with brine and dried over MgSO4. Crude Quinolin-3-ylmethanol was obtained upon filtration and concentration (795 mg; 86% yield).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US09067897B2 |
| Source dataset | uspto-grants-2015_06 |
| ORD ID | ord-f696dd7b7a684e56a1d93493111da2ad |
| Source note | uspto-grants-2015_06 |