HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 744091Generated: October 27, 2026
Dichloromethane → 1-[3,3-Bis(3-chlorophenyl)acryloyl]-4-(3,4-dimethoxybenzoyl)piperazine
https://huagongshe.com/reaction/744091
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Dichloromethane | HCID 6344 | — |
| Reactant | Veratric Acid | HCID 7121 | — |
| Reactant | P,P-Diphenylphosphinic azide | HCID 199401 | — |
| Reactant | 1-[3,3-Bis(3-chlorophenyl)acryloyl]piperazine | HCID 19421639 | — |
| Solvent | Triethylamine | HCID 8471 | — |
| Product | 1-[3,3-Bis(3-chlorophenyl)acryloyl]-4-(3,4-dimethoxybenzoyl)piperazine | HCID 19421655 | 94.6% |
Reaction Steps
0.44 ml of diphenylphosphoryl azide and 0.545 g of 1-[3,3-bis(3-chlorophenyl)acryloyl]piperazine (prepared as described in Preparation 111) were added to 10 ml of a methylene chloride solution containing 0.25 g of 3,4-dimethoxybenzoic acid and 0.38 ml of triethylamine, and the reaction mixture was stirred for 16 hours at room temperature. At the end of this time, the mixture was washed with 10% w/v aqueous hydrochloric acid, with a saturated aqueous solution of sodium bicarbonate and with water, in that order, after which it was dried over anhydrous sodium sulfate. The solvent was then removed by distillation under reduced pressure, and the resulting residue was purified by medium pressure chromatography using two Lobar B columns eluted with mixtures of hexane and ethyl acetate ranging from 1:2 to 1:4 by volume, to give 0.682 g of the title compound as a white powder.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05559109 |
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| Source dataset | uspto-grants-1996_09 |
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| ORD ID | ord-4b7b3aed20194f72b0e37cdac4fa5151 |
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| Source note | uspto-grants-1996_09 |
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