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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2100225Generated: November 1, 2026

Ethyl Acetate → HCID 87590877, compound

https://huagongshe.com/reaction/2100225

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthyl AcetateHCID 8857—
ReactantDi(succinimido) carbonateHCID 676246—
Reactant4-Amino-benzenesulfonic acid monosodium saltHCID 87136714—
SolventDimethyl SulfoxideHCID 679—
ProductHCID 87590877HCID 87590877115%

Reaction Steps

A solution of sodium sulfanilic acid (195 mg; 1 mmol) in dry DMSO (3 ml) was added dropwise to a solution of N,N′-disuccinimidyl carbonate (530 mg; 2 mmol) in dry DMSO (4 ml) and the resulting brownish solution stirred at room temperature for 20 hours. A solution of PAMAM 4.0 (EDA) (75 mg; 0.011 mmol) in dry DMSO (1 ml) added and the solution stirred for a further 18 hours. The solution was then concentrated under high vacuum (10−5 mmHg; 35°) to give a yellowish semi-solid. The crude product was dissolved in DMSO (4 ml) and the solution added to 200 ml of well stirred ethyl acetate. The precipitated white solid was collected by filtration and washed with ethyl acetate (2×) and ether (2×), then dried to give a white powder (275 mg). This material was further purified by gel filtration (Sephadex LH20; water) to give PAMAM 4.0 (EDA) terminated with 32 sodium 4-sulfophenylurea groups (106 mg). 1H nmr (D2O): δ2.31; 2.55; 2.75; 3.19; 7.32 (d, J=9 Hz); 7.63 (d, J=9 Hz). 13C nmr (D2O): δ36.3; 40.7; 43.3; 43.8; 53.7; 55.7; 123.3; 130.9; 140.9; 146.0; 161.4; 178.2; 178.6.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07572459B2
Source datasetuspto-grants-2009_08
ORD IDord-a3e509a2f3e7423bbf9a781b788c68d8
Source noteuspto-grants-2009_08