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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1932468Generated: November 4, 2026

Sodium borohydride → HCID 68524433, compound

https://huagongshe.com/reaction/1932468

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 numberUS08188277B2
Source datasetuspto-grants-2012_05
ORD IDord-c5a3fcef86dd42b7958e621169242a98
Source noteuspto-grants-2012_05