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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1771807Generated: November 2, 2026

Sodium borohydride → HCID 89443811, compound

https://huagongshe.com/reaction/1771807

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium borohydrideHCID 4311764—
Reactant3′,4-Difluoro[1,1′-biphenyl]-3-carboxaldehydeHCID 46312247—
ReactantHCID 82012920HCID 82012920—
SolventMethanolHCID 887—
SolventTolueneHCID 1140—
ProductHCID 89443811HCID 8944381185.8%

Reaction Steps

To a solution of 2-fluoro-5-(3-fluorophenyl)benzaldehyde (505 mg, 2.32 mmol, 1.2 eq) and 2-amino-3-fluoro-6-methoxy-benzonitrile (320 mg, 1.93 mmol, 1 eq) in toluene (30 mL) was added 4 Å molecular sieves (10 g). The mixture was heated at reflux for 4 h, then filtered to remove the molecular sieves. The filtrate was concentrated and the residue obtained was dissolved in methanol (30 mL). NaBH4 (109.6 mg, 2.9 mmol, 1.5 eq) was added and the reaction stirred for 2 h at room temperature. The reaction was quenched by addition of water, and the aqueous layer was extracted with EtOAc. The combined organic extracts were washed with brine, dried (Na2SO4), filtered and evaporated in vacuo. The residue obtained was purified by column chromatography (petroleum ether:EtOAc, 50:1) to give the title compound as an off-white solid (610 mg, 72%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09249085B2
Source datasetuspto-grants-2016_02
ORD IDord-88c98a9a917f43eaab3eeb1598336bd9
Source noteuspto-grants-2016_02