HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1532661Generated: November 1, 2026
4-Chloro-3-nitrobenzoic acid → 4-chloro-N-methyl-3-nitrobenzamide
https://huagongshe.com/reaction/1532661
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 4-Chloro-3-nitrobenzoic acid | HCID 7320 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | Thionyl Chloride | HCID 24386 | — |
| Reactant | Methylamine hydrochloride | HCID 6364545 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | 4-chloro-N-methyl-3-nitrobenzamide | HCID 799286 | — |
Reaction Steps
Thionyl chloride (0.65 ml) was added to a solution containing 4-chloro-3-nitrobenzoic acid (1.50 g) in N,N-dimethylformamide (15 ml) and stirred for 30 minutes at room temperature. Methylamine hydrochloride (1.21 g) and triethylamine (3.11 ml) were added to the reaction mixture. After being stirred for 1 hour at room temperature, the reaction mixture was concentrated. The residue, with ethyl acetate added thereto, was washed with water, 1N sodium hydroxide aqueous solution, 1N hydrochloric acid aqueous solution and saturated brine successively, dried over sodium sulfate anhydride, and concentrated. The yellow solid residue was purified by silica gel column chromatography (silica gel 10 g, chloroform:methanol=1:0-10:1), thereby yielding the entitled compound (0.97 g) as pale yellow solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06204264B1 |
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| Source dataset | uspto-grants-2001_03 |
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| ORD ID | ord-280327f4c0044d9bbcecb213aea13b42 |
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| Source note | uspto-grants-2001_03 |
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