Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 1-Nonanol | HCID 8914 | — |
| Reactant | 5-Hydroxy-2-pyrrolidone | HCID 194148 | — |
| Product | 5-n-Nonyloxy-pyrrolidin-2-one | HCID 15696566 | — |
Reaction Steps
A mixture of 5 g of 5-hydroxy-pyrrolidin-2-one 2.5 g of Amberlite IR 120H in 100 cm3 of n-nonanol is agitated at 60° C. for 3 hours. It is then cooled. the resin is filtered off, and the solvent is eliminated by distilling at 70° C. under 0.5 mbar. The residue is taken up in 50 cm3 of n-hexane, which is maintained for 16 hours at 5° C. After separating, 6.8 g of the expected product is obtained, m.p. 46°-48° C. After recrystallizing from n-hexane, m.p. 51°-52° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04882350 |
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| Source dataset | uspto-grants-1989_11 |
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| ORD ID | ord-26e2c2008b784df08462726627af4bc0 |
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| Source note | uspto-grants-1989_11 |
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