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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1814229Generated: October 31, 2026

Phthalimide → HCID 53485842, compound

https://huagongshe.com/reaction/1814229

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPhthalimideHCID 6809—
ReactantSodium CarbonateHCID 10340—
Reactant(-)-EpichlorohydrinHCID 2734062—
ReactantPotassium tert-butoxideHCID 23665647—
CatalystBenzyltrimethylammonium chlorideHCID 5963—
SolventIsopropanolHCID 3776—
ProductHCID 53485842HCID 5348584278%

Reaction Conditions

Temperature20 °C

Reaction Steps

Into a reaction vessel were put phthalimide (2.00 g, 13.6 mol), (R)-epichlorohydrin (2.52 g, 27.2 mol), anhydrous sodium carbonate (144 mg, 1.36 mol), benzyltrimethylammonium chloride (252 mg, 1.36 mol) and isopropanol (13 ml) and the mixture was reacted at room temperature for 15 hours. After removal unreacted epichlorohydrin, to the residue was added isopropanol (13 ml) and the mixture is cooled to 20° C. Then thereto was gradually dropped a mixture of potassium tert-butoxide (1.83 g, 16.3 mol) and isopropanol (7 ml) and the mixture was stirred for 1 hour at the same temperature. The solvent was removed and to the residue was added ethyl acetate (13 ml). The mixture was washed with water (7 ml), and then ethyl acetate was removed to give crude (R)-glycidylphthalimide (2.16 g, yield 78%, optical purity 98% e.e.) as white crystals.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06875875B2
Source datasetuspto-grants-2005_04
ORD IDord-58441e905e6e4ba1982a5d51f3e6000e
Source noteuspto-grants-2005_04