Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 2-Piperidone | HCID 12665 | — |
| Reactant | p-Toluenesulfonic acid monohydrate | HCID 521998 | — |
| Solvent | 1-Butanol | HCID 263 | — |
| Product | HCID 86740390 | HCID 86740390 | — |
Reaction Steps
Into a flask equipped with magnetic stirrer, thermometer, nitrogen inlet tube, and Dean-Stark trap were placed 25.0 parts of valerolactam (5-pentanelactam), 47.8 parts of para-toluenesulfonic acid monohydrate and 74.7 parts of butanol. The aforesaid mixture was placed under nitrogen atmosphere, heated to reflux to azeotropically remove any water present, and maintained at reflux until a constant acid value was attained. (The acid value was determined by the procedure described in Example I, above.) The reaction mixture was allowed to cool to 60° C. followed by the addition of 146.9 parts of methanol. The mixture was stirred and filtered to yield the [(4-butoxycarbonyl)butyl]ammonium tosylate. The aforesaid latent acid catalyst had a solids content of 30 percent in methanol and butanol.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04550137 |
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| Source dataset | uspto-grants-1985_10 |
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| ORD ID | ord-0ddaa60afeb2416b92e831a086616327 |
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| Source note | uspto-grants-1985_10 |
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