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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

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPhenyl glycidyl etherHCID 31217—
ReactantSodium MethoxideHCID 10942334—
ReactantN-[4-(piperazin-1-yl)phenyl]methanesulfonamide methanesulfonateHCID 86745083—
SolventMethanolHCID 887—
ProductN-[4-[4-(2-hydroxy-3-phenoxypropyl)piperazin-1-yl]phenyl]methanesulfonamideHCID 14739896—

Reaction Conditions

Temperature60 °C

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05051423
Source datasetuspto-grants-1991_09
ORD IDord-e08eaf4769d64f228a4ae5d48c13dfb2
Source noteuspto-grants-1991_09