HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2294141Generated: October 31, 2026
Dichloromethane → 3-(4-(2-Methoxyphenyl)piperazin-1-yl)propyl methanesulfonate
https://huagongshe.com/reaction/2294141
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Dichloromethane | HCID 6344 | — |
| Reactant | Sodium Carbonate | HCID 10340 | — |
| Reactant | Methanesulfonyl chloride | HCID 31297 | — |
| Reactant | 3-(4-(2-Methoxyphenyl)piperazin-1-yl)propan-1-ol | HCID 410901 | — |
| Solvent | Triethylamine | HCID 8471 | — |
| Product | 3-(4-(2-Methoxyphenyl)piperazin-1-yl)propyl methanesulfonate | HCID 10806184 | — |
Reaction Steps
A solution of 3-[4-(2-methoxyphenyl)piperazin-1-yl]-1-propanol (24 g, 95.87 mmol), prepared as in Example 10, in 25 mL of triethylamine and 300 mL of methylene chloride was cooled to approximately 0° C. and then methanesulfonyl chloride (8.8 mL) was added dropwise. The mixture was stirred at approximately 0° C. for 1 hour and then at room temperature for 0.5 hours. The mixture was poured into saturated sodium carbonate and stirred for 15 minutes. The organic phase was separated, washed with saturated sodium carbonate (2×150 mL), dried (MgSO4) and concentrated to give 3-[4-(2-methoxyphenyl)piperazin-1-yl]propyl methanesulfonate (21 g, 63.63 mmol).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05688795 |
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| Source dataset | uspto-grants-1997_11 |
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| ORD ID | ord-47bcbbe90e324b8a8821b5e288446cdd |
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| Source note | uspto-grants-1997_11 |
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