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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1479406Generated: November 2, 2026

Phthalimide → (E)-2-(3-(3,5-difluoro-4-phenoxyphenyl)-2-methylallyl)isoindoline-1,3-dione

https://huagongshe.com/reaction/1479406

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPhthalimideHCID 6809—
ReactantTriphenylphosphineHCID 11776—
Reactantethyl N-ethoxycarbonyliminocarbamateHCID 220568—
Reactant(E)-3-(3,5-difluoro-4-phenoxyphenyl)-2-methylprop-2-en-1-olHCID 67456176—
SolventTolueneHCID 1140—
SolventEthyl AcetateHCID 8857—
Product(E)-2-(3-(3,5-difluoro-4-phenoxyphenyl)-2-methylallyl)isoindoline-1,3-dioneHCID 6745894863%

Reaction Conditions

Temperature0 °C

Reaction Steps

To a solution of (E)-3-(3,5-difluoro-4-phenoxyphenyl)-2-methylprop-2-en-1-ol (Intermediate 93.1) (410 mg, 1.49 mmol) in dry toluene (7.45 mL) under N2 was added PPh3 and phthalimide. The resulting solution was cooled to 0° C. and diethyl azodicarboxylate (DEAD, 0.748 mL) was added dropwise over several minutes. The reaction was allowed to warm to room temperature and stirred overnight. After diluting with EtOAc (20 mL), the organic layer was washed with water (2×30 mL), brine (30 mL) and dried over Na2SO4. After removal of solvent, the resulting residue was applied to a silica gel column (15% EtOAc in hexanes) to yield 385 mg of the title compound (63%) as an oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09408840B2
Source datasetuspto-grants-2016_08
ORD IDord-1dbb6ce039c74d02b27e19f2eb67a30e
Source noteuspto-grants-2016_08