HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1904323Generated: November 2, 2026
1,2-Dichloroethane → HCID 14625129, compound
https://huagongshe.com/reaction/1904323
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 1,2-Dichloroethane | HCID 11 | — |
| Reactant | Water | HCID 962 | — |
| Reactant | Acetic acid, 2-(acetylthio)- | HCID 14485 | — |
| Reactant | 3-(3-(Piperidin-1-ylmethyl)phenoxy)propan-1-amine | HCID 10220561 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 14625129 | HCID 14625129 | — |
Reaction Steps
2.94 g of 3-{3-(piperidinomethyl)phenoxy}propylamine was dissolved in 80 ml of dichloromethane, and stirred under cooling in an ice bath. 1.60 g of 2-(acetylthio)acetic acid and 2.26 g of EDC were added to this solution, and stirred at 0° C. for 30 minutes then at room temperature overnight. 100 ml of water and 50 ml of dichloromethane were added to the reaction solution, and extraction was carried out. The dichloromethane layer was washed twice with water, and dried over anhydrous magnesium sulfate. The solvent was evaporated in vacuo, and the residue was purified by silica gel column chromatography using methanol:dichloromethane=1:15 as developing solvent to obtain the colorless oily N-[3-{3-(piperidinomethyl)phenoxy}propyl]-2-(acetylthio)acetamide. Yield: 2.23 g.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04837316 |
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| Source dataset | uspto-grants-1989_06 |
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| ORD ID | ord-9a69c6c3a46444bc8a50cce25ff383bd |
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| Source note | uspto-grants-1989_06 |
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