HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 353236Generated: October 29, 2026
O-Toluidine → N-(2-methylphenyl)-4-methylvaleramide
https://huagongshe.com/reaction/353236
Participants
| Role | Name | HCID | Charge |
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| Reactant | O-Toluidine | HCID 7242 | — |
| Reactant | Isocaproic acid | HCID 12587 | — |
| Reactant | 1,1'-Carbonyldiimidazole | HCID 68263 | — |
| Reactant | Isopentylindol | HCID 11041488 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | N-(2-methylphenyl)-4-methylvaleramide | HCID 22708317 | — |
Reaction Steps
Preparation of 2-(3-methyl-n-butyl)-indole. Carbonyldiimidazole (65 g) was mixed with 500 ml of dry dichloromethane in a 2-L round bottom flask and stirred magnetically. A solution of 4-methylvaleric acid in 200 ml of dichloromethane was added dropwise over 45 minutes and the mixture was stirred for another 1.25 hours. o-Toluidine (45 g) in 100 ml of dichloromethane was then added over about 20 minutes. After stirring for 2 hours the mixture was washed with water and then the solvent was stripped on a rotary evaporator. The residue was mixed with 150 ml of methanol and 75 ml of water and put in the freezer. Filtration of the precipitate, dilution of the filtrate with water and refiltration of the precipitate gave 75 g (94%) of vacuum dried N-(2-methylphenyl)-4-methylvaleramide which was used without further treatment in the next step.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06750240B2 |
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| Source dataset | uspto-grants-2004_06 |
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| ORD ID | ord-9ed715a2df7c47048f4b78f4d6d76603 |
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| Source note | uspto-grants-2004_06 |
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