HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 728829Generated: October 29, 2026
Phenyl glycidyl ether → N-[4-[4-(2-hydroxy-3-phenoxypropyl)piperazin-1-yl]phenyl]methanesulfonamide
https://huagongshe.com/reaction/728829
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Phenyl glycidyl ether | HCID 31217 | — |
| Reactant | Sodium Methoxide | HCID 10942334 | — |
| Reactant | N-[4-(piperazin-1-yl)phenyl]methanesulfonamide methanesulfonate | HCID 86745083 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | N-[4-[4-(2-hydroxy-3-phenoxypropyl)piperazin-1-yl]phenyl]methanesulfonamide | HCID 14739896 | — |
Reaction Steps
Suspend a mixture of 20.0 g (56.9 mmol) of N-[4-(piperazin-1-yl)phenyl]methanesulfonamide methanesulfonate, 7.68 mL (56.9 mmol) of 1,2-epoxy-3-phenoxypropane and 3.07 g (56.9 mmol) of sodiummethoxide in 800 mL of 90% aqueous methanol and warm to 60° C. for 18 h. After 18 h, filter the precipitate and wash this precipitate with 100 mL of water and 100 mL of methanol. Suspend this solid precipitate in 500 mL of methanol and reflux for 1 h. After 1 h, cool the suspension to room temperature and filter to obtain the title compound.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US05051423 |
|---|
| Source dataset | uspto-grants-1991_09 |
|---|
| ORD ID | ord-e08eaf4769d64f228a4ae5d48c13dfb2 |
|---|
| Source note | uspto-grants-1991_09 |
|---|