HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 35324Generated: October 29, 2026
Ethanol → N-(4-amino-2-methylphenyl)-2-chloroacetamide
https://huagongshe.com/reaction/35324
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Ethanol | HCID 702 | — |
| Reactant | Thiophene | HCID 8030 | — |
| Reactant | 2-chloro-N-(2-methyl-4-nitrophenyl)acetamide | HCID 352298 | — |
| Reactant | HCID 178418361 | HCID 178418361 | — |
| Catalyst | Platinum | HCID 23939 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | N-(4-amino-2-methylphenyl)-2-chloroacetamide | HCID 21295679 | 92% |
Reaction Steps
To 1 part of a solution of 2 parts of thiophene in 40 parts of ethanol were added 15 parts of 2-chloro-N-(2-methyl-4-nitrophenyl)acetamide and 400 parts of methanol. The whole was hydrogenated at normal pressure and at room temperature with 2 parts of platinum-on-charcoal catalyst 5%. After the calculated amount of hydrogen was taken up, the catalyst was filtered off and the filtrate was evaporated. The solid residue was purified by column-chromatography over silica gel using a mixture of trichloromethane and methanol (95:5 by volume) as eluent. The pure fractions were collected and the eluent was evaporated. The residue was suspended in 2,2'-oxybispropane. The product was filtered off and dried, yielding 12 parts (92%)of N-(4-amino-2-methylphenyl)-2-chloroacetamide (intermediate 70).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04766125 |
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| Source dataset | uspto-grants-1988_08 |
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| ORD ID | ord-9a978e6b54644696a6d3ec32141b02be |
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| Source note | uspto-grants-1988_08 |
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