Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Acetic Acid | HCID 176 | — |
| Reactant | Tetrahydropyran | HCID 8894 | — |
| Reactant | N-Hydroxyphthalimide | HCID 10665 | — |
| Product | Glutaric Acid | HCID 743 | 11% |
| Product | Glutaric anhydride | HCID 7940 | 9% |
| Product | Delta-Valerolactone | HCID 10953 | 28% |
Reaction Steps
A mixture of 3 mmole of tetrahydropyran, 10 mole % of N-hydroxyphthalimide relative to tetrahydropyran, 0.5 mole % of acetylacetonatocobalt(II) Co(AA)2 relative to tetrahydropyran, and 5 ml of acetic acid was stirred for 15 hours at 60° C. under an oxygen atmosphere. The products in the reaction mixture were analyzed by gas chromarography, and, as a result, tetrahydropyran was converted into δ-valerolactone (yield 28%), glutaric acid (yield 11%) and glutaric anhydride (yield 9%) with a conversion of 67%.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06037477 |
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| Source dataset | uspto-grants-2000_03 |
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| ORD ID | ord-3198ad5cce7e4f9fbead0f4d0814794d |
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| Source note | uspto-grants-2000_03 |
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