HuagongsheHuagongshe Chemistry Print Report · For research reference only
6-Aminohexanoic Acid → 6-Aminohexanoic Acid
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 6-Aminohexanoic Acid | HCID 564 | — |
| Reactant | Nonanoyl chloride | HCID 69819 | — |
| Product | 6-Aminohexanoic Acid | HCID 564 | — |
| Product | Nonanoyl chloride | HCID 69819 | — |
| Product | Hexanoic acid, 6-[(1-oxononyl)amino]- | HCID 11022006 | — |
Reaction Steps
N-nonanoyl-6-aminocaproic acid was prepared by reaction of nonanoyl chloride with 6-aminocaproic acid according to the procedure described in Example I. From 67.3 g (0.381 mol) of nonanoyl chloride and 50.0 g (0.381 mol) of 6-aminocaproic acid was obtained 103 g of N-nonanoyl-6-aminocaproic acid, mp 71°-74° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04634551 |
| Source dataset | uspto-grants-1987_01 |
| ORD ID | ord-f8bde2f8c91d4b4c9ed5db484bf39870 |
| Source note | uspto-grants-1987_01 |