Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1814722Generated: October 27, 2026

Benzaldehyde, 4-(diphenylamino)- → (4-(Diphenylamino)phenyl)methanol

https://huagongshe.com/reaction/1814722

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzaldehyde, 4-(diphenylamino)-HCID 77846—
ReactantSodium borohydrideHCID 4311764—
SolventEthanolHCID 702—
SolventSodium HydroxideHCID 14798—
Product(4-(Diphenylamino)phenyl)methanolHCID 1132333992%

Reaction Steps

The compound (1) obtained in Example 1-1, that is, 4-(diphenylamino)benzaldehyde, (4.2 g) was dissolved in 50 mL of ethanol and a solution prepared by dissolving 0.29 g of NaBH4 in 0.1 M aqueous solution of NaOH (15 mL) was slowly added thereto. The reactant solution was reacted at room temperature for 4 hours. An organic layer was separated from the reactant solution using methylene chloride and recrystallized in a methylene chloride/hexane solvent, yielding 92% of a white solid. Data of NMR spectra confirmed that the product had the same structure as the compound (2) in the reaction scheme 2.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06878468B2
Source datasetuspto-grants-2005_04
ORD IDord-0546ba01bb7942039b91eeaf8d2accaa
Source noteuspto-grants-2005_04