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
Participants
| Role | Name | HCID | Charge |
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| Reactant | Toluene-4-sulfonic acid tetrahydro-furan-3-ylmethyl ester | HCID 15335290 | — |
| Reactant | Phthalimide potassium salt | HCID 24194345 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | 2-[(Oxolan-3-yl)methyl]-1H-isoindole-1,3(2H)-dione | HCID 22399030 | — |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08026359B2 |
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| Source dataset | uspto-grants-2011_09 |
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| ORD ID | ord-3ec3dab14f2a4574ba3e843825dff5c2 |
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| Source note | uspto-grants-2011_09 |
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