HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 217104Generated: October 30, 2026
Poly-gamma-benzyl L-glutamate → HCID 21197492, compound
https://huagongshe.com/reaction/217104
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Poly-gamma-benzyl L-glutamate | HCID 95441 | — |
| Reactant | Potassium Bromide | HCID 253877 | — |
| Reactant | HCID 17998586 | HCID 17998586 | — |
| Solvent | Hydrogen Bromide | HCID 260 | — |
| Product | HCID 21197492 | HCID 21197492 | — |
Reaction Steps
2-Amino-5-(benzyloxy)-5-oxopentanoic acid, 20.00 g (0.084 mole), and potassium bromide, 34.1 g (0.29 mole), were dissolved in 80 mL of ˜6N aqueous HBr, previously chilled to 0° C. A stream of nitrogen was bubbled through the solution and the mixture was chilled to −10° C. by means of a cold bath. Sodium nitrite, 6.98 g (0.10 mole) was added in portions over 30 min with stirring, while maintaining the temperature of the reaction from −13° C. to −10° C. After 6 hours stirring at −10° C., the mixture was extracted with ethyl ether, 4×100 mL and the resulting solution dried with magnesium sulfate. The mixture was filtered to remove the drying agent and evaporated to give an orange oil. The oil was purified by flash chromatography, chloroform-hexanes to give a clear and colorless oil. The yield was 11.5 g, i.e., 45%, based on starting 2-amino-{[(benzyl-oxy)-5-oxopentanoic acid. NMR is consistent with structure.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08193347B2 |
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| Source dataset | uspto-grants-2012_06 |
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| ORD ID | ord-b5033bfb9aeb4f5ea7b726dfc34b9411 |
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| Source note | uspto-grants-2012_06 |
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