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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1620288Generated: November 1, 2026

Sodium borohydride → (2-methylquinolin-6-yl)methanol

https://huagongshe.com/reaction/1620288

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium borohydrideHCID 4311764—
Reactant2-methylquinoline-6-carbaldehydeHCID 7537486—
SolventTetrahydrofuranHCID 8028—
Product(2-methylquinolin-6-yl)methanolHCID 2795481105.1%

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08772316B2
Source datasetuspto-grants-2014_07
ORD IDord-749a0a61be634611adbb132d86c4acae
Source noteuspto-grants-2014_07