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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2080140Generated: October 30, 2026

Phthalimide → 2-(5-(2-Cyclopropylvinyl)thiophen-2-ylmethyl)isoindol-1,3-dione

https://huagongshe.com/reaction/2080140

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPhthalimideHCID 6809—
ReactantTriphenylphosphineHCID 11776—
ReactantAzodicarboxylic acid dimethyl esterHCID 351621—
Reactant(5-(2-Cyclopropylvinyl)thiophen-2-yl)methanolHCID 67119677—
SolventWaterHCID 962—
SolventTetrahydrofuranHCID 8028—
Product2-(5-(2-Cyclopropylvinyl)thiophen-2-ylmethyl)isoindol-1,3-dioneHCID 6711958320.6%

Reaction Steps

(5-(2-Cyclopropylvinyl)thiophen-2-yl)methanol described in Preparation Example 149 (930 mg, 5.19 mmol), triphenylphosphine (2040 mg, 7.78 mmol) and phthalimide (1140 mg, 7.78 mmol) were dissolved in tetrahydrofuran (50 mL), azodicarboxylic acid dimethyl ester (1140 mg, 7.78 mmol) was added under stirring at room temperature, and the solution was stirred for 1 hour. Water (50 mL) was added to the reaction solution, which was then extracted with ethyl acetate (50 mL). The organic layer was washed with water, dried over anhydrous magnesium sulfate, and the solvent was evaporated in vacuo. The residue was purified by NH silica gel column chromatography (hexane:ethyl acetate=9:1), and the title compound (330 mg, 1.07 mmol, 20.6%) was obtained as a white solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07932272B2
Source datasetuspto-grants-2011_04
ORD IDord-2d298c00649e4899b21c8af722e2b048
Source noteuspto-grants-2011_04