HuagongsheHuagongshe Chemistry Print Report · For research reference only
4-Methyl-L-glutamate → gamma-methyl-L-glutamic acid gamma-hexyl-L-glutamic acid
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 4-Methyl-L-glutamate | HCID 440959 | — |
| Reactant | gamma-hexyl-L-glutamic acid | HCID 86718962 | — |
| Product | gamma-methyl-L-glutamic acid gamma-hexyl-L-glutamic acid | HCID 86718961 | — |
Reaction Steps
The synthesized copolymer (10 mg) was dissolved in deuterated trifluoroacetic acid, and the 1H NMR was measured. As a result, a peak derived from the methyl group of γ-methyl-L-glutamic acid was detected near 3.8 ppm, and a peak derived from the proton at the α-position of γ-methyl-L-glutamic acid and γ-hexyl-L-glutamic acid was detected near 4.7 ppm. When peak area near 3.8 ppm is A and that near 4.7 ppm is B, A/B=1.17. Since A/B=3.00 for poly-γ-methyl-L-glutamic acid, the decreased portion is considered to be substituted by a hexyl group. Therefore, the content percentage of the hexyl group is 61% since 1.83/3.00=0.61. Hence, the composition of the copolymer is γ-methyl-L-glutamic acid (39%)/γ-hexyl-L-glutamic acid (61%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US09450174B2 |
| Source dataset | uspto-grants-2016_09 |
| ORD ID | ord-2421fb0b2bf94f1195d8862a868d39a2 |
| Source note | uspto-grants-2016_09 |