Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1904323Generated: November 2, 2026

1,2-Dichloroethane → HCID 14625129, compound

https://huagongshe.com/reaction/1904323

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1,2-DichloroethaneHCID 11—
ReactantWaterHCID 962—
ReactantAcetic acid, 2-(acetylthio)-HCID 14485—
Reactant3-(3-(Piperidin-1-ylmethyl)phenoxy)propan-1-amineHCID 10220561—
SolventDichloromethaneHCID 6344—
ProductHCID 14625129HCID 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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04837316
Source datasetuspto-grants-1989_06
ORD IDord-9a69c6c3a46444bc8a50cce25ff383bd
Source noteuspto-grants-1989_06