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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 850272Generated: October 27, 2026

L-Aspartic Acid → Ninhydrin

https://huagongshe.com/reaction/850272

Reaction equation

Participants

RoleNameHCIDCharge
ReactantL-Aspartic AcidHCID 5960—
ReactantL-Glutamic AcidHCID 33032—
ReactantN-alpha-tert-Butyloxycarbonylglutamic acid gamma-fluorenylmethyl esterHCID 129966—
ReactantN-alpha-tert-Butyloxycarbonyl-aspartic acid gamma-fluorenylmethyl esterHCID 164019—
ProductNinhydrinHCID 10236—

Reaction Steps

This methodology uses Nα -Boc-amino acids together with OFm side-chain protection for Asp and Glu. Asp and Glu were introduced with Boc-Asp(OFm)-OH and Boc-Glu(OFm)-OH. After coupling the last amino acid, the OFm protecting groups were selectively removed by treating the peptide resin in 50% piperidine in DMF (Dimethylformamide) for 1 h. The peptide resin was washed with DMF (3×40 mL), DCM (dicholoromethane) (3×40 mL), suspended in 15 mL of DMF, and mixed with a 6-fold excess of BOP reagent in the presence of an 8-fold excess of diisopropylamine (DIEA) for 5 h. The coupling was repeated until the resin gave the negative ninhydrin test.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06017877
Source datasetuspto-grants-2000_01
ORD IDord-f994617829bf4f45b55582893ddba8c3
Source noteuspto-grants-2000_01