Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 62236Generated: October 25, 2026

p-Toluenesulfonic acid → (E)-2-((1-benzylpiperidin-4-yl)methylene)-6-methoxy-5-morpholino-2,3-dihydro-1H-inden-1-one

https://huagongshe.com/reaction/62236

Reaction equation

Participants

RoleNameHCIDCharge
Reactantp-Toluenesulfonic acidHCID 6101—
Reactant1-Benzylpiperidine-4-carbaldehydeHCID 89584—
Reactant6-Methoxy-5-morpholino-2,3-dihydro-1H-inden-1-oneHCID 117940128—
SolventTolueneHCID 1140—
SolventEthyl AcetateHCID 8857—
Product(E)-2-((1-benzylpiperidin-4-yl)methylene)-6-methoxy-5-morpholino-2,3-dihydro-1H-inden-1-oneHCID 117940242—

Reaction Conditions

Temperature120 °C

Reaction Steps

To a solution of 13 (150 mg, 0.607 mmol) in toluene 15 mL was added 1-benzylpiperidine-4-carbaldehyde 21 (123.4 mg, 0.607 mmol). p-Toluene sulphonic acid (PTSA) (230.9 mg, 1.214 mmol) was added to the reaction mixture, and stirred at 120° C. for 6 h. The reaction mass was diluted with ethyl acetate and washed with water (3×25 mL). The organic layer was dried over sodium sulphate and concentrated to get the crude material, which was purified through flash chromatography using 100-200 mesh silica gel. Eluting at 30% ethyl acetate in hexane gave yellow coloured solid (E)-2-((1-benzylpiperidin-4-yl)methylene)-6-methoxy-5-morpholino-2, 3-dihydro-1H-inden-1-one 22.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09446047B2
Source datasetuspto-grants-2016_09
ORD IDord-5de892651a514d5ca22c4e338408d1f5
Source noteuspto-grants-2016_09