HuagongsheHuagongshe Chemistry Print Report · For research reference only
Heptanenitrile, 7-amino- → N~1~-Propylheptane-1,7-diamine
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Heptanenitrile, 7-amino- | HCID 31676 | — |
| Reactant | Propionyl chloride | HCID 62324 | — |
| Reactant | HCID 19028721 | HCID 19028721 | — |
| Reactant | Aluminium lithium hydride | HCID 21226445 | — |
| Reactant | N-(6-Cyanohexyl)propanamide | HCID 21452875 | — |
| Solvent | Benzene | HCID 241 | — |
| Solvent | Pyridine | HCID 1049 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | N~1~-Propylheptane-1,7-diamine | HCID 21452856 | — |
Reaction Steps
The intermediate N-n-propyl-1,7-heptanediamine was prepared in two steps following the procedure described in Example 119. There was first obtained, as an amber liquid, 14.4 g. of 7-propionamidoheptanonitrile using 10.0 g. of 7-aminoheptanonitrile, 8.1 g. of propionyl chloride, 6.9 g. of pyridine and 100 ml. of benzene. Next was obtained 9.3 g. of n-propyl-1,7-heptanediamine, b.p. 112°-116° C. at 5 mm., using 8.0 g. of lithium aluminum hydride in 900 ml. of tetrahydrofuran and 18.2 g. of 7-propionamidoheptanonitrile in 100 ml. of tetrahydrofuran.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04009208 |
| Source dataset | uspto-grants-1977_02 |
| ORD ID | ord-a337065dd3cf46e3aebf5d7dfcbbd398 |
| Source note | uspto-grants-1977_02 |