HuagongsheHuagongshe Chemistry Print Report · For research reference only
6-Aminohexanoic Acid → 6-Acrylamidohexanoic Acid
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 6-Aminohexanoic Acid | HCID 564 | — |
| Reactant | L-Glutamic Acid | HCID 33032 | — |
| Product | 6-Acrylamidohexanoic Acid | HCID 324200 | 85% |
Reaction Steps
Using the same procedure as previously described except substituting 6-aminocaproic acid for the glutamic acid, the crude product was obtained in greater than 85% yield. After crystallization from water or ethyl acetate, the white, crystalline N-acryloyl-6-aminocaproic acid had a melting point of 88°-90° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05369142 |
| Source dataset | uspto-grants-1994_11 |
| ORD ID | ord-6a45d20a31cc43349cd1305a55ab7015 |
| Source note | uspto-grants-1994_11 |