Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Cyclopentanol | HCID 7298 | — |
| Reactant | 87710-47-2 | HCID 353549 | — |
| Product | HCID 19838069 | HCID 19838069 | — |
Reaction Steps
A mixture of 4.5 g of 1,5-dihydro-5-hydroxy-2H-pyrrol-2-one, 100 cm3 of cyclopentanol and 2.25 g of Amberlite IR 120 H is maintained for 8 hours at 60° C. It is then allowed to cool, is filtered, and evaporated to dryness. The residue is chromatographed on silica (eluent: ethyl acetate-n-hexane, 1--1). 3 g of the expected product is obtained, m.p.=77°-78° C. crystallized from cyclohexane. After recrystallizing from a mixture of isopropyl ether-n-hexane, 1--1, m.p.=81°-82° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04885307 |
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| Source dataset | uspto-grants-1989_12 |
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| ORD ID | ord-4f261d3d0f1d435d9d465e96d36835f4 |
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| Source note | uspto-grants-1989_12 |
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