HuagongsheHuagongshe Chemistry Print Report · For research reference only
Ammonia → Acrylamide, N-cyclohexyl-
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Ammonia | HCID 222 | — |
| Reactant | Cyclohexylamine | HCID 7965 | — |
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | 3-Methoxypropanamide | HCID 5252481 | — |
| Product | Acrylamide, N-cyclohexyl- | HCID 137811 | — |
Reaction Steps
103.1 g (1.0 mole) of 3-methoxypropionamide are heated with 104.1 g (1.05 mole) of cyclohexylamine for 8 hours in a temperature range of 130°-170° C. until the evolution of ammonia is complete. The mixture is allowed to cool, 1.5 g of sodium hydroxide is added and the mixture is heated in a high vacuum at 90°-110° C. The methanol is split off within about 30 minutes, vigorous foaming occurring. The temperature is increased and 93.5 g (0.61 mole=61% of the theoretical yield) of N-cyclohexylacrylamide having a Bp0.1 of 124°-128° C., which solidifies into crystalline form in the receiver, are distilled off.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04237067 |
| Source dataset | uspto-grants-1980_12 |
| ORD ID | ord-bd65b2df867f48398120a128bcecd266 |
| Source note | uspto-grants-1980_12 |