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
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 3,4,5,6-Tetrahydrophthalic anhydride | HCID 12475 | — |
| Reactant | Potassium tert-butoxide | HCID 23665647 | — |
| Reactant | HCID 87671437 | HCID 87671437 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 69312050 | HCID 69312050 | — |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09283222B2 |
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| Source dataset | uspto-grants-2016_03 |
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| ORD ID | ord-668219fa247942afa0f5cf40ce3f66cf |
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| Source note | uspto-grants-2016_03 |
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