HuagongsheHuagongshe Chemistry Print Report · For research reference only
Ammonia → Allylamine
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Ammonia | HCID 222 | — |
| Reactant | Triallylamine | HCID 7617 | — |
| Reactant | Allyl Alcohol | HCID 7858 | — |
| Reactant | 1,3-Propanediol | HCID 10442 | — |
| Reactant | 1,4-Bis(diphenylphosphino)butane | HCID 82124 | — |
| Catalyst | Palladium Chloride | HCID 24290 | — |
| Solvent | Water | HCID 962 | — |
| Product | Allylamine | HCID 7853 | — |
| Product | Diallylamine | HCID 31279 | — |
Reaction Steps
To 1.8 mg (0.01 millimole) of PdCl2 was added 8.5 mg (0.02 millimole) of 1,4-bis(diphenylphosphino)butane, and 5.0 g of 1,3-propane-diol and 3.6 g of water were added and reaction between 8.4 g (145 millimoles) of allyl alcohol and 3.2 g (188 millimoles) of ammonia was carried out at 110° C. with stirring for 2 hours. As the products, there were obtained 0.26 g (4.6 millimoles) of monoallylamine, 0.53 g (5.4 millimoles) of diallylamine 0.63 g (4.6 millimoles) of triallylamine. The conversion based on allyl alcohol was 21.5% and the selectivity was 96.8%.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04942261 |
| Source dataset | uspto-grants-1990_07 |
| ORD ID | ord-692e55a0d76041d3a7e1aa34e763b27d |
| Source note | uspto-grants-1990_07 |