Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 902584Generated: October 26, 2026

L-Aspartic Acid → (5-dibutylamino-naphthalene-1-sulfonyl)-L-aspartic acid

https://huagongshe.com/reaction/902584

Reaction equation

Participants

RoleNameHCIDCharge
ReactantL-Aspartic AcidHCID 5960—
ReactantBansyl compoundHCID 191102—
ReactantSodium BicarbonateHCID 516892—
SolventAcetoneHCID 180—
SolventWaterHCID 962—
Product(5-dibutylamino-naphthalene-1-sulfonyl)-L-aspartic acidHCID 69279796—

Reaction Steps

Two mmoles of aspartic acid and 4 mmoles of NaHCO3 were dissolved in 5 ml of water. A solution containing 1 mmol of 5-dibutylamino-naphthalene-1-sulfonyl chloride (Bansyl chloride, Purchased from TCI) in acetone was slowly added. More acetone was added until the solution was clear. The mixture was stirred overnight at room temperature and protected from light. Acetone was removed by flash evaporation and the remaining water solution was acidified to a of pH=4.5 to 5 by adding 2M citric acid. Then, NaCl was added until saturation and the solution was extracted with three portions of ethyl acetate (20 ml each). Extracts were combined, dried over MgSO4 and the solution was filtered. The solvent was removed and the residue was purified by liquid chromatography on a silica gel. A gradient of 0 to 5% methanol in dichloromethane was used as eluent. Fractions containing the desired product were combined and solvents removed. The residue was triturated in 1:1 ether: petroleum ether. The precipitate was filtered out and dried in vacuum overnight thus affording 5-dibutylamino-naphthalene-1-sulfonyl)-L-aspartic acid (NST705).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07365223B2
Source datasetuspto-grants-2008_04
ORD IDord-bcd6dae67d894c5891d5e8382fd42bf3
Source noteuspto-grants-2008_04