HuagongsheHuagongshe Chemistry Print Report · For research reference only
Hydrochloric Acid → 4-{1-[4-Acetoxy-5-(4-tert-butylphenyl)thiphen-3-yl]ethylidenehydrazinocarbonyl}-2-nitro benzoic acid
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Water | HCID 962 | — |
| Reactant | 4-Hydrazinocarbonyl-2-nitrobenzoic acid | HCID 67050297 | — |
| Reactant | Acetic acid 4-acetyl-2-(4-tert-butylphenyl)thiophen-3-yl ester | HCID 67050465 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | 4-{1-[4-Acetoxy-5-(4-tert-butylphenyl)thiphen-3-yl]ethylidenehydrazinocarbonyl}-2-nitro benzoic acid | HCID 57804352 | 28% |
Reaction Steps
To a solution of acetic acid 4-acetyl-2-(4-tert-butylphenyl)thiophen-3-yl ester (63.3 mg, 0.2 mmol) and 4-hydrazinocarbonyl-2-nitrobenzoic acid (54.0 mg, 0.24 mmol) in DMF (1 mL) was added 12 M aqueous HCl solution (16.7 μL, 0.2 mmol). The reaction mixture was stirred overnight, and then water was added. The precipitated solid was collected by filtration and washed with water and CHCl3 to give product as a pale yellow solid (29.1 mg, yield 28%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07576115B2 |
| Source dataset | uspto-grants-2009_08 |
| ORD ID | ord-d39222faf83945ee9fe7f10b81e6f821 |
| Source note | uspto-grants-2009_08 |