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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1935422Generated: November 3, 2026

Methyl p-toluenesulfonate → N-[1-(S)-[alpha-(R)-methoxybenzyl)-3-methyl-butyl]phthalimide

https://huagongshe.com/reaction/1935422

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethyl p-toluenesulfonateHCID 6645—
ReactantSodium hydrideHCID 24758—
ReactantN-[1-(S)-[alpha-(R)-hydroxybenzyl]-3-methylbutyl]phthalimideHCID 12087153—
SolventTolueneHCID 1140—
ProductN-[1-(S)-[alpha-(R)-methoxybenzyl)-3-methyl-butyl]phthalimideHCID 18741230—

Reaction Steps

To a solution of N-[1-(S)-[α-(R)-hydroxybenzyl]-3-methylbutyl]phthalimide (30.4 g, 94.0 mmol.) in toluene (380 mL) were successively added methyl p-toluenesulfonate (19.2 g, 103 mmol.) and 60% sodium hydride (4.13 g, 103 mmol.). The resulting mixture was heated under reflux for 18 hours under stirring, cooled to room temperature, successively washed with water and aqueous saturated sodium chloride solution, dried over anhydrous sodium sulfate. The solvent was distilled off under reduced pressure. The residue was purified by middle pressure column chromatography (n-hexane/ethyl acetate=5/1), to give N-[1-(S)-[α-(R)-methoxybenzyl]-3-methylbutyl]phthalimide as a white crystalline product (25.6 g, yield: 81%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06387908B1
Source datasetuspto-grants-2002_05
ORD IDord-db7dc8ea1cbe4d0b9401ea7af0ffc30e
Source noteuspto-grants-2002_05