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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2270138Generated: November 1, 2026

Ethanol → HCID 70213064, compound

https://huagongshe.com/reaction/2270138

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthanolHCID 702—
ReactantEthyl nitroacetateHCID 69379—
ReactantSodium AcetateHCID 517045—
Reactantmethyl 4-amino-2-(N-tert-butylsulfamoyl)benzoateHCID 10946074—
ReactantSodium NitriteHCID 23668193—
SolventHydrochloric AcidHCID 313—
SolventWaterHCID 962—
ProductHCID 70213064HCID 7021306460%

Reaction Steps

5.7 g (0.02 mol) of methyl 4-amino-2-(N-tert-butylsulfamoyl)benzoate are suspended in a mixture of 30 ml of conc. HCl and 36 ml of water. At 0-50° C., a solution of 1.5 g (0.022 mol) of sodium nitrite in 9 ml of water is added dropwise. The few undissolved components are filtered off cold, and the cold diazonium salt solution is slowly poured, at 5-10° C., into a mixture of 8.9 g (0.11 mol) of sodium acetate, 16 ml of water, 60 ml of ethanol and 2.7 g (0.02 mol) of ethyl nitroacetate. Stirring is continued at 0° C. for 2 h and the mixture is left to stand at this temperature for 15 h. The mixture is filtered off and the solid is washed with water and dried under reduced pressure, giving 5.2 g (60% of theory) of methyl 2-(N-tert-butylsulfamoyl)-4-(ethoxycarbonylnitromethylenehydrazino)benzoate of m.p. 142-145° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06331506B1
Source datasetuspto-grants-2001_12
ORD IDord-14973849024c40909c96f3d5c191a3a3
Source noteuspto-grants-2001_12