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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2074518Generated: October 30, 2026

Sodium borohydride → (5-Chloro-2-(2-(trifluoromethyl)phenyl)quinolin-3-yl)methanol

https://huagongshe.com/reaction/2074518

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium borohydrideHCID 4311764—
Reactant5-Chloro-2-(2-(trifluoromethyl)phenyl)quinoline-3-carbaldehydeHCID 57556183—
SolventTetrahydrofuranHCID 8028—
Product(5-Chloro-2-(2-(trifluoromethyl)phenyl)quinolin-3-yl)methanolHCID 67090613—

Reaction Conditions

Temperature0 °C

Reaction Steps

To a solution of 5-chloro-2-(2-(trifluoromethyl)phenyl)quinoline-3-carbaldehyde (2.1673 g, 6.456 mmol) in 32 mL of THF at 0° C. was added sodium borohydride (0.3664 g, 9.684 mmol) and the mixture was stirred at 0° C. After 1 hr at 0° C., the mixture was partitioned between EtOAc (100 mL) and H2O (100 mL), and the organic layer was washed with brine (50 mL×3), dried over Na2SO4, filtered, and concentrated under reduced pressure to give (5-chloro-2-(2-(trifluoromethyl)phenyl)quinolin-3-yl)methanol as a yellow syrup: 1H NMR (400 MHz, DMSO-d6) δ ppm 8.68-8.73 (1 H, m), 7.96-8.02 (1 H, m), 7.90-7.95 (1 H, m), 7.83-7.87 (1 H, m), 7.68-7.83 (3 H, m), 7.50-7.58 (1 H, m), 5.63 (1 H, t, J=5.3 Hz), 4.36 (2 H, br. s.); LC-MS (ESI) m/z 338.0 [M+H]+. The product was carried on crude without purification for the next step.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07919498B2
Source datasetuspto-grants-2011_04
ORD IDord-20b9747a3e4b47ae81d1a6a1d3a25aa9
Source noteuspto-grants-2011_04