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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 236261Generated: October 25, 2026

N-3-Bromopropylphthalimide → N-[3-(3-piperidinomethylphenoxy)propyl]phthalimide

https://huagongshe.com/reaction/236261

Reaction equation

Participants

RoleNameHCIDCharge
ReactantN-3-BromopropylphthalimideHCID 21611—
ReactantSodium hydrideHCID 24758—
Reactant1-(3-Hydroxybenzyl)piperidineHCID 826974—
SolventDimethylformamideHCID 6228—
ProductN-[3-(3-piperidinomethylphenoxy)propyl]phthalimideHCID 1289856588.6%

Reaction Steps

In 150 ml of N,N-dimethylformamide was suspended 4.8 g of sodium hydride (52% purity), and 20.0 g of 3-piperidinomethylphenol was added in small portions with stirring under ice-cooling. After the addition, the resulting mixture was subjected to reaction at room temperature for 1 hour. To the reaction mixture thus obtained was added 28.0 g of N-(3-bromopropyl)phthalimide, and the resulting mixture was subjected to reaction for 24 hours. After completion of the reaction, the solvent was removed by distillation under reduced pressure, and 300 ml of water and 300 ml of chloroform were added to the resulting residue to dissolve the same. The organic layer was separated and then dried over anhydrous magnesium sulfate, after which the solvent was removed by distillation under reduced pressure to obtain 35.0 g (yield 88.5%) of oily N-[3-(3-piperidinomethylphenoxy)propyl]phthalimide.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04643849
Source datasetuspto-grants-1987_02
ORD IDord-7b74214388e8488c8bf929a13e7fbba7
Source noteuspto-grants-1987_02