HuagongsheHuagongshe Chemistry Print Report · For research reference only
Sodium borohydride → (2-methylquinolin-6-yl)methanol
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Sodium borohydride | HCID 4311764 | — |
| Reactant | 2-methylquinoline-6-carbaldehyde | HCID 7537486 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | (2-methylquinolin-6-yl)methanol | HCID 2795481 | 105.1% |
Reaction Steps
To a stirred solution of 2-methylquinoline-6-carbaldehyde (1.00 g, 5.8 mmol) in THF (60 mL) in a 100 mL round-bottomed flask equipped with a magnetic stirrer was added NaBH4 (0.221 g, 5.8 mmol) and the mixture was stirred overnight at RT then cooled in an ice bath before quenching by addition of a 1 N aq. HCl solution (10 mL). After stirring for 15 min at RT, the mixture was basified to pH=9 with a 2 N aq. NaOH solution. THF was then removed at 40° C. under vacuum and the solution was extracted with CH2Cl2 (200 mL), washed with brine (20 mL), dried over Na2SO4, filtered and concentrated under vacuum to give (2-methylquinolin-6-yl)methanol SLA 47080A as a yellow oil (1.056 g, quant.).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08772316B2 |
| Source dataset | uspto-grants-2014_07 |
| ORD ID | ord-749a0a61be634611adbb132d86c4acae |
| Source note | uspto-grants-2014_07 |