HuagongsheHuagongshe Chemistry Print Report · For research reference only
2-Chloro-3-quinolinecarboxaldehyde → (2-Chloroquinolin-3-yl)methanol
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 2-Chloro-3-quinolinecarboxaldehyde | HCID 690958 | — |
| Reactant | Sodium borohydride | HCID 4311764 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | (2-Chloroquinolin-3-yl)methanol | HCID 930708 | — |
Reaction Steps
A suspension of 2-chloro-3-quinolinecarbaldehyde (19.2 g, 100 mmol) in methanol (400 ml) is treated with sodium borohydride (5.7 g, 150 mmol). After agitation for 2 hours at ambient temperature, the reaction medium is concentrated under reduced pressure then taken up in water, filtered, washed with water and with ethanol in order to produce, after drying under reduced pressure, 15.8 g (81%) of a white solid, m.p. 166° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06436951B1 |
| Source dataset | uspto-grants-2002_08 |
| ORD ID | ord-5f6161128e4045928e69e9f91c8f9598 |
| Source note | uspto-grants-2002_08 |