Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Ammonia | HCID 222 | — |
| Reactant | Cyclohexylamine | HCID 7965 | — |
| Reactant | 3-Hydroxypropanamide | HCID 4145140 | — |
| Product | Acrylamide, N-cyclohexyl- | HCID 137811 | — |
Reaction Steps
59 g of β-hydroxypropionamide and 69.4 g of cyclohexylamine were heated with 50 mg of 2,6-di-t-butyl-pcresol for 5 hours in a temperature range of 130°-170° C. until the evolution of ammonia was complete. After adding 2.5 g of polyphosphoric acid the reaction mixture was maintained at 164° C. for 1 hour and then distilled in a water jet vacuum. The main run was taken off between 140° and 160° C. at 11 bar and crystallized in the receiver.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04237067 |
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| Source dataset | uspto-grants-1980_12 |
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| ORD ID | ord-2affe934e98d48669833c62c048622d8 |
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| Source note | uspto-grants-1980_12 |
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