HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 655641Generated: October 29, 2026
Methanol → 1-Benzo[b]thiophen-4-yl-4-(3-chloropropyl)piperazine
https://huagongshe.com/reaction/655641
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Methanol | HCID 887 | — |
| Reactant | Carbon Tetrachloride | HCID 5943 | — |
| Reactant | Triphenylphosphine | HCID 11776 | — |
| Reactant | 3-(4-Benzo[b]thiophen-4-yl-piperazin-1-yl)propanol | HCID 57482548 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | 1-Benzo[b]thiophen-4-yl-4-(3-chloropropyl)piperazine | HCID 57482551 | — |
Reaction Steps
3.56 g (12.9 mmol) of 3-(4-benzo[b]thiophen-4-yl-piperazin-1-yl)propan-1-ol was suspended in 30 ml of dichloromethane, and carbon tetrachloride (30 ml) and triphenyl phosphine (4.06 g, 15.5 mmol) were added thereto. The mixture was refluxed with heating for 3 hours. The reaction solution was cooled to room temperature, then methanol and dichloromethane were added thereto to homogenize the mixture. Silica gel (30 g) was added to the solution, and the solvent was evaporated under reduced pressure. The obtained residue was loaded on silica gel column (300 g) and extracted with a solvent mixture of n-hexane:ethyl acetate=2:1. The extraction solution was concentrated under reduced pressure to obtain 1-benzo[b]thiophen-4-yl-4-(3-chloropropyl)piperazine (2.36 g) as colorless oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US08071600B2 |
|---|
| Source dataset | uspto-grants-2011_12 |
|---|
| ORD ID | ord-52edf86f6148474bb4651c8effb6e48a |
|---|
| Source note | uspto-grants-2011_12 |
|---|