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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 496102Generated: October 30, 2026

Ethylenediaminetetraacetic Acid → 5-Acetyl-2-aminobenzenesulfonamide

https://huagongshe.com/reaction/496102

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthylenediaminetetraacetic AcidHCID 6049—
ReactantEthyl vinyl etherHCID 8023—
ReactantSodium HydroxideHCID 14798—
Reactant2-Amino-5-iodobenzenesulfonamideHCID 22324088—
ReactantHCID 178418306HCID 178418306—
CatalystZincchlorideHCID 3007855—
CatalystHCID 178418397HCID 178418397—
SolventTetrahydrofuranHCID 8028—
SolventHexaneHCID 8058—
Product5-Acetyl-2-aminobenzenesulfonamideHCID 1295239974%

Reaction Conditions

Temperature-78 °C

Reaction Steps

To a solution of ethylvinylether (5.8 ml, 60 mmol) in dry THF (50 ml) at −78° C. was added t-BuLi (1.7 M in pentane, 25 ml, 40 mmol) and the yellow mixture was stirred for 1 h at −78° C. The cooling bath was removed and the mixture was warmed slowly to 0° C. and stirred for another 30 min. The mixture was recooled to −78° C. and a solution of ZnCl2 (2M in THF, 20 ml, 40 mmol) was added slowly and the cooling bath was removed and warmed to 20° C. 5-Iodo-2-aminobenzenesulfonamide (see compound 37) (1.8 g, 6 mmol) and Pd(PPh3)4 (0.2 g, 3 mol %) was added and the mixture was refluxed for 6 h. The THF was evaporated and the residue was boiled in 1 M hydrochloric acid (30 ml) and MeOH (30 ml) for 30 min. EDTA (14.6 g, 50 mmol) was added and made slightly basic (pH=8-9) with 1 M NaOH followed by extraction with EtOAc (3×150 ml), drying (Na2SO4) and evaporation of the solvent gave a brown solid. Trituration with n-hexane gave 0.95 g (74%) of 5-acetyl-2-aminobenzenesulfonamide as off-white powder. The product was further transformed by Method G (using cyclohexanecarboxaldehyde). M.p. 224-226° C. (decomp).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06943159B1
Source datasetuspto-grants-2005_09
ORD IDord-d882de079fe840589a1adccd40227bc2
Source noteuspto-grants-2005_09