HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 655666Generated: October 29, 2026
Dichloromethane → HCID 57499597, compound
https://huagongshe.com/reaction/655666
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Dichloromethane | HCID 6344 | — |
| Reactant | Acetyl chloride | HCID 6367 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | HCID 53630738 | HCID 53630738 | — |
| Solvent | Water | HCID 962 | — |
| Product | HCID 57499597 | HCID 57499597 | 66% |
Reaction Steps
Triethylamine (0.28 ml, 2.0 mmol) was added to a dichloromethane solution (15 ml) of 1-benzo[b]thiophen-4-yl-4-[3-(piperidin-4-yloxy)-propyl]-piperazine (0.45 g, 1.25 mmol) and the mixture was cooled in an ice bath. To this, acetyl chloride (0.1 ml, 1.4 mmol) was added and the mixture was stirred at room temperature overnight. Water was added to the reaction solution, which was then extracted with dichloromethane. The organic layer was dried over anhydrous sodium sulfate and thereafter concentrated under reduced pressure. The residue was purified by silica gel column chromatography (dichloromethane:methanol=30:1). The purified product was concentrated under reduced pressure. To the residue, 0.5 N hydrochloride-methanol solution (3 ml) was added. The crystal produced was obtained by filtration and dried to obtain 1-benzo[b]thiophen-4-yl-4-[3-(1-acetylpiperidin-4-yloxy)propyl]piperazine hydrochloride as white powder (0.36 g, 66% yield).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US08071600B2 |
|---|
| Source dataset | uspto-grants-2011_12 |
|---|
| ORD ID | ord-d2b251faa5684e73a8f98f8a076d8be0 |
|---|
| Source note | uspto-grants-2011_12 |
|---|