HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 347398Generated: October 27, 2026
1-Chloro-4-nitrobenzene → N-(4-Chlorophenyl)acetamide
https://huagongshe.com/reaction/347398
Participants
| Role | Name | HCID | Charge |
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| Reactant | 1-Chloro-4-nitrobenzene | HCID 7474 | — |
| Reactant | HCID 178418634 | HCID 178418634 | — |
| Catalyst | Potassium Carbonate | HCID 11430 | — |
| Product | N-(4-Chlorophenyl)acetamide | HCID 10871 | 91% |
Reaction Steps
In one example, under nitrogen gas, a stirred mixture of 4-Chloro-1-nitrobenzene (e.g., about 1 g, 6.35 mmol), thioacetic acid (e.g., about 1.93 g, 25.39 mmol), K2CO3 (e.g., about 0.050 g, 0.36 mmol), and dry Triton-X 405 (e.g., about 0.010 g) were heated at about 150° C. The progress of the reaction was monitored by HPLC and GC. After four hours the reaction was cooled to room temperature, and acetone (e.g., about 8 mL) was added and filtered through a sintered glass funnel. Evaporation of the acetone produced about 0.975 g of N-(4-Chloro-phenyl)-acetamide (e.g., about 91%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07173152B2 |
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| Source dataset | uspto-grants-2007_02 |
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| ORD ID | ord-61da0582113a45c69fa1cfe0f8661d35 |
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| Source note | uspto-grants-2007_02 |
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