HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 584915Generated: October 26, 2026
Dimethyl malonate → HCID 22341500, compound
https://huagongshe.com/reaction/584915
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Dimethyl malonate | HCID 7943 | — |
| Reactant | Piperidine, acetate | HCID 9793820 | — |
| Reactant | N-(4'-formylbiphenyl-3-ylmethyl)-N-methylbenzamide | HCID 22341491 | — |
| Solvent | Toluene | HCID 1140 | — |
| Product | HCID 22341500 | HCID 22341500 | — |
Reaction Steps
1.54 g (4.25 mmol) of N-(4′-formylbiphenyl-3-ylmethyl)-N-methylbenzamide (prepared as in Example 1(e)), 20 ml of toluene, 0.56 g (4.25 mmol)) of dimethyl malonate and 123 mg (0.85 mmol) of piperidine acetate are introduced into a three-necked flask under a stream of nitrogen. The mixture is refluxed for 5 hours, while separating off the water formed using Dean-Stark apparatus. The reaction medium is cooled, extracted with ethyl acetate and washed with water. The organic phase is separated out after settling of the phases has taken place, dried over magnesium sulfate and evaporated. The crude product is purified by chromatography on a column of silica eluted with a mixture of heptane and ethyl acetate (70/30). After evaporation of the solvents, 1.4 g (75%) of the expected product are collected.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06927228B2 |
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| Source dataset | uspto-grants-2005_08 |
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| ORD ID | ord-d5e90e8e9ae9433ca134dcaddb8ee651 |
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| Source note | uspto-grants-2005_08 |
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