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
Participants
| Role | Name | HCID | Charge |
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| Reactant | p-Toluenesulfonic acid | HCID 6101 | — |
| Reactant | 1-Benzylpiperidine-4-carbaldehyde | HCID 89584 | — |
| Reactant | 6-Methoxy-5-morpholino-2,3-dihydro-1H-inden-1-one | HCID 117940128 | — |
| Solvent | Toluene | HCID 1140 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | (E)-2-((1-benzylpiperidin-4-yl)methylene)-6-methoxy-5-morpholino-2,3-dihydro-1H-inden-1-one | HCID 117940242 | — |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09446047B2 |
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| Source dataset | uspto-grants-2016_09 |
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| ORD ID | ord-5de892651a514d5ca22c4e338408d1f5 |
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| Source note | uspto-grants-2016_09 |
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