HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 64527Generated: October 25, 2026
Bicyclo(2.2.1)heptane-2-methanol → gamma-benzyl-L-glutamic acid gamma-2-norbornylmethyl-L-glutamic acid
https://huagongshe.com/reaction/64527
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Bicyclo(2.2.1)heptane-2-methanol | HCID 21308 | — |
| Reactant | L-Glutamic Acid | HCID 33032 | — |
| Reactant | p-Toluenesulfonic acid monohydrate | HCID 521998 | — |
| Solvent | 1,2-Dichloroethane | HCID 11 | — |
| Product | gamma-benzyl-L-glutamic acid gamma-2-norbornylmethyl-L-glutamic acid | HCID 131737227 | — |
Reaction Steps
By a method similar to that of Synthetic Example 4, poly-γ-benzyl-L-glutamic acid was obtained and dissolved in 1,2-dichloroethane. Thereto were added an equivalent amount of norbornane-2-methanol (manufactured by Tokyo Chemical Industry Co., Ltd.) relative to the glutamic acid unit of poly-γ-benzyl-L-glutamic acid and a catalytic amount of p-toluenesulfonic acid monohydrate, and the mixture was stirred at 65° C. for 4 days to give a γ-benzyl-L-glutamic acid/γ-2-norbornylmethyl-L-glutamic acid copolymer. The weight average molecular weight, Mw, of the obtained copolymer was measured by Measurement Method 1 described below. In addition, the composition of the polymer after transesterification reaction was measured by Measurement Method 2 described below.
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-4ac422f9d7e546669ce56ede6c3f5b19 |
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| Source note | uspto-grants-2016_09 |
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