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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

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPoly-gamma-benzyl L-glutamateHCID 95441—
ReactantPotassium BromideHCID 253877—
ReactantHCID 17998586HCID 17998586—
SolventHydrogen BromideHCID 260—
ProductHCID 21197492HCID 21197492—

Reaction Conditions

Temperature0 °C

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08193347B2
Source datasetuspto-grants-2012_06
ORD IDord-b5033bfb9aeb4f5ea7b726dfc34b9411
Source noteuspto-grants-2012_06