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
Participants
| Role | Name | HCID | Charge |
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| Reactant | Phenylacetic Acid | HCID 999 | — |
| Reactant | Dicyclohexylcarbodiimide | HCID 10868 | — |
| Reactant | methyl 2-(N-tert-butylsulfamoyl)-4-hydrazinobenzoate | HCID 21716182 | — |
| Catalyst | 4-(Dimethylamino)pyridine | HCID 14284 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | Methyl 2-(N-tert-butylsulfamoyl)-4-(2-phenylacetylhydrazino)benzoate | HCID 53894777 | — |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05849666 |
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| Source dataset | uspto-grants-1998_12 |
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| ORD ID | ord-9a03cf7953de43f692f15e8c305b3e35 |
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| Source note | uspto-grants-1998_12 |
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