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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2171343Generated: November 1, 2026

Sodium borohydride → (4-((6-Chloropyridin-3-yl)oxy)-3-fluorophenyl)methanol

https://huagongshe.com/reaction/2171343

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium borohydrideHCID 4311764—
Reactant4-((6-Chloropyridin-3-yl)oxy)-3-fluorobenzaldehydeHCID 86724192—
SolventMethanolHCID 887—
Product(4-((6-Chloropyridin-3-yl)oxy)-3-fluorophenyl)methanolHCID 86676396—

Reaction Conditions

Temperature25 °C

Reaction Steps

To a solution of 4-((6-chloropyridin-3-yl)oxy)-3-fluorobenzaldehyde (2.80 g, 11.1 mmol) in methanol (25 mL) was added portionwise solid NaBH4 (0.842 g, 22.3 mmol) at room temperature. The reaction mixture was stirred at 25° C. for 2 h, concentrated to remove solvent, dissolved in water (50 mL) and extracted with ethyl acetate (50 mL×2). Combined organic parts were washed with brine, dried over anhydrous Na2SO4, filtered and concentrated. The crude was used into next step without purification (2.8 g).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09051325B2
Source datasetuspto-grants-2015_06
ORD IDord-b27902b7a0314f36aa75815c99f5066a
Source noteuspto-grants-2015_06