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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 913295Generated: October 31, 2026

Toluene-4-sulfonic acid tetrahydro-furan-3-ylmethyl ester → 2-[(Oxolan-3-yl)methyl]-1H-isoindole-1,3(2H)-dione

https://huagongshe.com/reaction/913295

Reaction equation

Participants

RoleNameHCIDCharge
ReactantToluene-4-sulfonic acid tetrahydro-furan-3-ylmethyl esterHCID 15335290—
ReactantPhthalimide potassium saltHCID 24194345—
SolventDimethylformamideHCID 6228—
Product2-[(Oxolan-3-yl)methyl]-1H-isoindole-1,3(2H)-dioneHCID 22399030—

Reaction Conditions

Temperature80 °C

Reaction Steps

To a solution of (tetrahydro-3-furanyl)methyl 4-methylbenzenesulfonate (i.e., the product of Step A) (11.0 g, 42.9 mmol) in N,N-dimethylformamide (160 mL) was added potassium phthalimide (7.9 g, 42.7 mmol) in one portion, and the resulting mixture was stirred at 80° C. for 6 h. Additional potassium phthalimide (5 g, 27 mmol) was added, and stirring was continued at 100° C. for 18 h. The cooled reaction mixture was partitioned between water and ethyl acetate and the aqueous layer was separated and extracted with ethyl acetate (5×75 mL). The combined extracts were dried over MgSO4 and filtered, and the solvent was removed under reduced pressure to give a residue which was chromatographed on silica gel (40 g) eluted with 5% to 100% ethyl acetate in hexanes to give 4.5 g of the title compound as a white solid, m.p. 114-118° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08026359B2
Source datasetuspto-grants-2011_09
ORD IDord-3ec3dab14f2a4574ba3e843825dff5c2
Source noteuspto-grants-2011_09