Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 2-Pyrrolidone | HCID 12025 | — |
| Reactant | p-Toluenesulfonic acid monohydrate | HCID 521998 | — |
| Solvent | 1-Butanol | HCID 263 | — |
| Product | HCID 86740391 | HCID 86740391 | — |
Reaction Steps
Into a reactor flask equipped with magnetic stirrer, thermometer, nitrogen inlet tube, and Dean-Stark trap were placed 47.0 parts of 2-pyrrolidinone (4-butanelactam), 109.4 parts of para-toluenesulfonic acid monohydrate, and 197.4 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 280.8 parts of methanol over a five-minute period. The mixture was stirred and filtered to yield the [(3-butoxycarbonyl)propyl]ammonium tosylate. The aforesaid latent acid catalyst had a solids content of 30 percent in methanol and isobutanol.
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-cbb1cda1aea446c8b947bf99dd76e69d |
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| Source note | uspto-grants-1985_10 |
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