Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 15704Generated: October 30, 2026

Water → HCID 23014682, compound

https://huagongshe.com/reaction/15704

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantAnilineHCID 6115—
ReactantSodium borohydrideHCID 4311764—
Reactant2-(1-Indenyl)benzaldehydeHCID 13023488—
SolventEthanolHCID 702—
SolventTolueneHCID 1140—
ProductHCID 23014682HCID 2301468271.1%

Reaction Steps

To a solution of 2-(1-indenyl)benzaldehyde (7.0 mmol) in ethanol (19.4 mL) was added dropwise aniline (7.3 mmol) under a nitrogen atmosphere. The mixture was stirred at room temperature. After disappearance of the aldehyde was confirmed by gas chromatography, The solvent was distilled off under reduced pressure. After addition of ethanol (19.4 mL), sodium borohydride (4.5 mmol) was added to the solution and the mixture was reacted at room temperature for 3 hrs. Water and toluene were then added to the reaction mixture. The organic layer was dried and concentrated. The obtained oily substance was purified by silica gel column chromatography to give N-[2-(1-indenyl)phenylmethyl]-N-phenylamine (1.48 g, yield 24.0%) as a yellow oily substance.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07732643B2
Source datasetuspto-grants-2010_06
ORD IDord-e7450ae0d3dd42d2955cb45fe1c4c29e
Source noteuspto-grants-2010_06