HuagongsheHuagongshe Chemistry Print Report · For research reference only
Ammonia → Didodecylamine
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Ammonia | HCID 222 | — |
| Reactant | Dodecylamine | HCID 13583 | — |
| Reactant | HCID 178418361 | HCID 178418361 | — |
| Product | Didodecylamine | HCID 18157 | — |
Reaction Steps
The same procedure as in Example 13 was repeated except for using the catalyst (K) produced in Preparation Example 10 in place of the catalyst (G), flowing ammonia and hydrogen through the autoclave at rates of 13.1 g (0.77 mol)/h and 4.3 L (0.19 mol)/h, respectively, thereby conducting the reaction for 6 h. The resultant reaction product was analyzed in the same manner as in Example 7. As a result, it was confirmed that the conversion of the raw alcohol was 65.5%, the selectivity to lauryl amine was 85.5%, the amount of dilauryl amine produced is 7.3%, and the amount of the other by-products produced was 2.2%.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08247611B2 |
| Source dataset | uspto-grants-2012_08 |
| ORD ID | ord-756c3c24d30a41f9917cef02b1a84144 |
| Source note | uspto-grants-2012_08 |