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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 232164Generated: October 30, 2026

HCID 13935580, compound → N-(4-benzyloxy-3,3-difluorobutyl)phthalimide

https://huagongshe.com/reaction/232164

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHCID 13935580HCID 13935580—
ReactantPhthalimide potassium saltHCID 24194345—
SolventDimethylformamideHCID 6228—
ProductN-(4-benzyloxy-3,3-difluorobutyl)phthalimideHCID 13935581—

Reaction Conditions

Temperature100 °C

Reaction Steps

A mixture of 1-benzyloxy-2,2-difluoro-4-methanesulfonyloxybutane (63.44 g, 0.216 moles), potassium phthalimide (44 g, 0.238 moles) and dry DMF (500 mL), distilled from CaH2) is stirred and heated at 100° C. After a short time the mixture solidifies, and an additional dry DMF (500 mL) is added. Upon heating at 90°-100° C. for another 20 hours, salts are removed by filtration, and the DMF is distilled under vacuum (oil pump). The residue is dissolved in CH2Cl2 (800 mL) and washed with 1N KOH (twice) and 1N HCl (twice). Drying (Na2SO4) and evaporation yields N-(4-benzyloxy-3,3-difluorobutyl)-phthalimide as a yellow oil: 68.5 g (92%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04851448
Source datasetuspto-grants-1989_07
ORD IDord-51c51fb0e110471eb6de3df94ff1f508
Source noteuspto-grants-1989_07