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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1259289Generated: October 31, 2026

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

https://huagongshe.com/reaction/1259289

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 numberUS08466150B2
Source datasetuspto-grants-2013_06
ORD IDord-7c5e27f3ad20430abf65c1a7aefca52f
Source noteuspto-grants-2013_06