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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1721420Generated: November 3, 2026

Benzaldehyde → HCID 22414827, compound

https://huagongshe.com/reaction/1721420

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzaldehydeHCID 240—
ReactantBenzeneHCID 241—
ReactantSodium cyanoborohydrideHCID 5003444—
Reactant5-Ethoxy-2-methylanilineHCID 23369755—
SolventWaterHCID 962—
ProductHCID 22414827HCID 22414827—

Reaction Steps

100 ml of benzene was added to 20.8 g (138 mmol) of 2-amino-4-ethoxytoluene and 17.8 g (168 mmol) of benzaldehyde, and the mixture was heated with refluxing for 5 hours in a reaction vessel equipped with a water separator. After cooling, the reaction solution was concentrated under reduced pressure. 640 ml of methanol was added to the residue, followed by the addition of acetic acid to adjust pH to 5. To this was added 13.1 g (208 mmol) of sodium cyanoborohydride while stirring under cooling with ice, and the mixture was stirred overnight at room temperature. The reaction mixture was concentrated, purified by column chromatography (silica gel, chloroform), and recrystallized (chloroform-n-hexane) to obtain 19.7 g (yield, 59.2%) of colorless prisms of the title compound.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05510366
Source datasetuspto-grants-1996_04
ORD IDord-f649f13e6d204d9390fe1a251f919559
Source noteuspto-grants-1996_04