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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2230754Generated: October 30, 2026

Ethyl Acetate → HCID 87590877, compound

https://huagongshe.com/reaction/2230754

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthyl AcetateHCID 8857—
ReactantDi(succinimido) carbonateHCID 676246—
Reactant515-74-2HCID 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 numberUS06426067B1
Source datasetuspto-grants-2002_07
ORD IDord-2403e4df63e140dc81759556df70b191
Source noteuspto-grants-2002_07