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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 884116Generated: October 31, 2026

Sodium borohydride → HCID 68524433, compound

https://huagongshe.com/reaction/884116

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium borohydrideHCID 4311764—
ReactantHCID 68525979HCID 68525979—
SolventMethanolHCID 887—
ProductHCID 68524433HCID 68524433—

Reaction Steps

Methyl 4-{5-[(4-trifluoromethylbenzylidene)-amino]pyridin-2-yloxy}benzoate (2.64 g, 6.59 mmol) was suspended in methanol (25 mL), and to the resulting suspension was slowly added sodium borohydride (1.25 g, 33.0 mmol). The resulting solution was stirred at room temperature for 3 days. The reaction solution was concentrated under reduced pressure. To the residue was added ethyl acetate, and washed with water and brine. The organic layer was dried over anhydrous magnesium sulfate, and evaporated. The residue was washed with diethyl ether, to thereby yield 2.65 g of the title compound.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08236826B2
Source datasetuspto-grants-2012_08
ORD IDord-257934ffaeb24c418a2858b8c93e85c1
Source noteuspto-grants-2012_08