HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 989782Generated: October 29, 2026
Dichloromethane → N-piperidinopropyl-5-(3,4-dichlorophenyl)-3-methyl-pentadiene carboxamide
https://huagongshe.com/reaction/989782
Participants
| Role | Name | HCID | Charge |
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| Reactant | Dichloromethane | HCID 6344 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | Isobutyl chloroformate | HCID 62365 | — |
| Reactant | Piperidino-propylamine | HCID 18419402 | — |
| Reactant | 5-(3,4-dichlorophenyl)-3-methyl-pentadienoic Acid | HCID 85811893 | — |
| Product | N-piperidinopropyl-5-(3,4-dichlorophenyl)-3-methyl-pentadiene carboxamide | HCID 88175739 | — |
Reaction Steps
A suspension of 5-(3,4-dichlorophenyl)-3-methyl-pentadienoic acid (0.100 g, 0.390 mmol) in CH2Cl2 (5 mL) is treated with triethyl-amine (0.050 cr, 0.050 mmol) and cooled to 0° C. The resulting colorless solution is then treated with isobutyl chloroformate (0.065 g, 0.050 mmol). After 30 min., piperidino-propylamine (0.071 g, 0.050 mmol) is added, and the reaction mixture is allowed to warm to room temperature. After stirring overnight, the reaction mixture is quenched with aqueous sodium bicarbonate. The aqueous layer is extracted several times with CH2Cl2, and the combined organic layers are dried (sodium sulfate), and concentrated in vacuo. The residue is treated with excess methanolic HCl, evaporated in vacuo, and rinsed with ether to yield 0.159 g of a hygroscopic white solid, mp 50-60° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06458806B1 |
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| Source dataset | uspto-grants-2002_10 |
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| ORD ID | ord-b67944bef1b641c29bb85de48b76ef73 |
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| Source note | uspto-grants-2002_10 |
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