HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2108101Generated: October 27, 2026
Triethylamine → 1-(3-Coumarinylcarbonyl)-4-(3,4,5-trimethoxybenzyl)piperazine
https://huagongshe.com/reaction/2108101
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | Coumarin-3-Carboxylic Acid | HCID 10752 | — |
| Reactant | Diethyl cyanophosphonate | HCID 76257 | — |
| Reactant | 1-[(3,4,5-Trimethoxyphenyl)methyl]piperazine;dihydrochloride | HCID 12828501 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Solvent | Hexane | HCID 8058 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | 1-(3-Coumarinylcarbonyl)-4-(3,4,5-trimethoxybenzyl)piperazine | HCID 14849702 | 16.9% |
Reaction Steps
To a mixture of coumarin-3-carboxylic acid (0.9 g), 1(3,4,5-trimethoxybenzyl)piperazine dihydrochloride (1.7 g), triethylamine (1.8 g) and N,N-dimethylformamide (20 ml) is added dropwise at room temperature diethyl cyanophosphonate (1.8 ml), followed by stirring for one hour. After addition of water (50 ml), the reaction mixture is left standing for 30 minutes, followed by addition of water (150 ml), ethyl acetate (200 ml) and hexane (50 ml). The mixture is vigorously mixed and the organic layer is separated. The organic layer is washed with water, dried, and concentrated under reduced pressure. The residue is purified by means of a silica gel column chromatography(hexane:acetone=1:1-1:2) to give an oily product, which is crystallized from a mixture of acetone and ethyl ether to afford 1-(3-coumarinylcarbonyl)-4-(3,4,5-trimethoxybenzyl)piperazine (0.35 g) as colorless needles, m.p. 171°-173° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04937246 |
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| Source dataset | uspto-grants-1990_06 |
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| ORD ID | ord-2fb59b6ff0f84f86af51d2af3a2b22a0 |
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| Source note | uspto-grants-1990_06 |
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