HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1968937Generated: October 31, 2026
Ethanol → N-(3-chloro-4-fluorophenyl)-4-methylbenzamide
https://huagongshe.com/reaction/1968937
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Ethanol | HCID 702 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | Ammonium Chloride | HCID 25517 | — |
| Reactant | N-(3-chloro-4-fluorophenyl)-4-methyl-3-nitrobenzamide | HCID 710855 | — |
| Catalyst | Iron | HCID 23925 | — |
| Solvent | Water | HCID 962 | — |
| Product | N-(3-chloro-4-fluorophenyl)-4-methylbenzamide | HCID 710613 | 117.1% |
Reaction Steps
0.7 g of the product of Step 1 was added into 80 ml of ethanol:water (v/v=31), then 1.0 g iron powder and 0.4 g ammonium chloride. After addition, the reaction mixture was heated to 70° C. and reacted for 30 min. The completion of reaction was indicated by TLC. The reaction mixture was filtered, and the filter cake was washed with hot ethanol repeatedly. Then the filtrate was concentrated under reduced pressure to give a white solid. Then 20 ml potassium carbonate solution (10%) was added into the solid. The mixture was stirred, left to stand, filtered, and dried to give a light yellow solid (0.7 g).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US08426446B2 |
|---|
| Source dataset | uspto-grants-2013_04 |
|---|
| ORD ID | ord-ea0c9244a5254fab920761172bc75e8c |
|---|
| Source note | uspto-grants-2013_04 |
|---|