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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 925075Generated: October 30, 2026

3,4,5,6-Tetrahydrophthalic anhydride → HCID 69312050, compound

https://huagongshe.com/reaction/925075

Reaction equation

Participants

RoleNameHCIDCharge
Reactant3,4,5,6-Tetrahydrophthalic anhydrideHCID 12475—
ReactantPotassium tert-butoxideHCID 23665647—
ReactantHCID 87671437HCID 87671437—
SolventTetrahydrofuranHCID 8028—
ProductHCID 69312050HCID 69312050—

Reaction Conditions

Temperature0 °C

Reaction Steps

A suspension of EXAMPLE 285B (1.88 g, 3.4 mmol) in tetrahydrofuran (100 ml) was treated with potassium t-butoxide (1N solution in tetrahydrofuran, 3.4 ml, 3.4 mmol) at −78° C. for 1 hour, and was allowed to warm up to 0° C. over 30 minutes. A solution of 4,5,6,7-tetrahydroisobenzofuran-1,3-dione (0.54 g, 3.4 mmol) in tetrahydrofuran (10 ml) was then added. The reaction mixture was warmed up to room temperature, and stirred at room temperature for additional 4 hours. After quenching with water, the reaction mixture was partitioned between ethyl acetate and brine. The organic phase was washed with brine, and concentrated. The residue was separated by flash chromatography (20% ethyl acetate in hexane) to provide the title compound. MS (DCI/NH3) m/z 320 (M+H)+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09283222B2
Source datasetuspto-grants-2016_03
ORD IDord-668219fa247942afa0f5cf40ce3f66cf
Source noteuspto-grants-2016_03