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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1457521Generated: October 25, 2026

Phenylacetic Acid → Methyl 2-(N-tert-butylsulfamoyl)-4-(2-phenylacetylhydrazino)benzoate

https://huagongshe.com/reaction/1457521

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPhenylacetic AcidHCID 999—
ReactantDicyclohexylcarbodiimideHCID 10868—
Reactantmethyl 2-(N-tert-butylsulfamoyl)-4-hydrazinobenzoateHCID 21716182—
Catalyst4-(Dimethylamino)pyridineHCID 14284—
SolventDichloromethaneHCID 6344—
ProductMethyl 2-(N-tert-butylsulfamoyl)-4-(2-phenylacetylhydrazino)benzoateHCID 53894777—

Reaction Conditions

Temperature25 °C

Reaction Steps

1.5 g (7.3 mmol) of dicyclohexylcarbodiimide (DCC) are added to a solution of 2.0 g (6.6 mmol) of methyl 2-(N-tert-butylsulfamoyl)-4-hydrazinobenzoate, 0.9 g (6.6 mmol) of phenylacetic acid and 0.03 g of 4-dimethylaminopyridine (DMAP) in 20 ml of CH2Cl2 at 0° C. The mixture is stirred at 25° C. for 15 hours, the solid is filtered off with suction and the organic phase is washed successively with water, 1N HCl and NaHCO3 solution, dried and evaporated. This gives 1.6 g (58% of theory) of methyl 2-(N-tert-butylsulfamoyl)-4-(2-phenylacetyl-hydrazino)benzoate with the following nuclear magnetic resonance data:

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05849666
Source datasetuspto-grants-1998_12
ORD IDord-9a03cf7953de43f692f15e8c305b3e35
Source noteuspto-grants-1998_12