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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1690318Generated: October 30, 2026

Benzaldehyde → 8-(Phenylmethylidene)-5,6,7,8-tetrahydroquinoline

https://huagongshe.com/reaction/1690318

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzaldehydeHCID 240—
Reactant5,6,7,8-TetrahydroquinolineHCID 66335—
SolventAcetic AnhydrideHCID 7918—
Product8-(Phenylmethylidene)-5,6,7,8-tetrahydroquinolineHCID 5407465058%

Reaction Steps

Benzaldehyde (3.59 mL, 35.30 mmole) was added to a solution of 5,6,7,8-tetrahydro-quinoline (4.70 g, 35.30 mmole) in acetic anhydride (25 mL), and the solution was heated to reflux under a nitrogen atmosphere. After overnight at reflux, the reaction was concentrated in vacuo. The residue was diluted with water and extracted with ethyl acetate. The combined organic extracts were washed with brine, dried over Na2SO4, and concentrated. The residue was purified by flash chromatography on silica gel (33% EtOAc/hexanes) to give the title compound (4.50 g, 58%) as a waxy yellow solid after drying in vacuo: MS (ES) m/e 222 (M+H)+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08153652B2
Source datasetuspto-grants-2012_04
ORD IDord-b3519e8cba864d51941a05a8a1f815b4
Source noteuspto-grants-2012_04