HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 64533Generated: October 26, 2026
epsilon-(Benzyloxycarbonyl)-L-lysine → gamma-benzyl-L-glutamic acid Nepsilon-benzyloxycarbonyl-L-lysine
https://huagongshe.com/reaction/64533
Participants
| Role | Name | HCID | Charge |
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| Reactant | epsilon-(Benzyloxycarbonyl)-L-lysine | HCID 1715626 | — |
| Reactant | gamma-benzyl-L-glutamic acid | HCID 22787902 | — |
| Product | gamma-benzyl-L-glutamic acid Nepsilon-benzyloxycarbonyl-L-lysine | HCID 86718960 | — |
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 benzyl group of Nε-benzyloxycarbonyl-L-lysine and the benzyl group of γ-benzyl-L-glutamic acid was detected near 5.1 ppm, a peak derived from the proton at the α-position of γ-benzyl-L-glutamic acid was detected near 4.7 ppm, and a peak derived from the proton at the α-position of Nε-benzyloxycarbonyl-L-lysine was detected near 4.4 ppm. When the peak areas near 5.1 ppm, 4.7 ppm, 4.4 ppm are A, B, C, respectively, A/B=4.00, A/C=4.00, and B/C=1.00. Since both B and C represent an area of one proton, the composition of the copolymer is γ-benzyl-L-glutamic acid (50%)/Nε-benzyloxycarbonyl-L-lysine (50%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09450174B2 |
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| Source dataset | uspto-grants-2016_09 |
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| ORD ID | ord-d2361c97e90743c2bd9752cc01be3734 |
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| Source note | uspto-grants-2016_09 |
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