HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2188495Generated: November 1, 2026
Triethylamine → 4-nitro-N-(2,4,4-trimethylpentan-2-yl)benzamide
https://huagongshe.com/reaction/2188495
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | 4-Nitrobenzoyl chloride | HCID 8502 | — |
| Reactant | tert-Octylamine | HCID 61017 | — |
| Solvent | 1,1-Dichloroethane | HCID 6365 | — |
| Product | 4-nitro-N-(2,4,4-trimethylpentan-2-yl)benzamide | HCID 698029 | 76% |
Reaction Steps
tert-Octylamine (51.7 g, 0.4 mol) and triethyamine (61.2 ml, 0.44 mol) are introduced into 260 ml of dichloroethane in a reactor. The mixture is heated to 70° C. and then 4-nitrobenzoyl chloride (77.9 g, 0.42 mol) is added in small portions over 50 minutes. The mixture is heated at reflux for 4 hours. The mixture is poured onto ice-cold water; extraction is carried out with dichloromethane, the extract is dried and the solvent is evaporated. The beige precipitate obtained is recrystallized from a mixture of isopropyl ether and ethanol (ratio 10:1). After drying under vacuum, 84.6 g (Yield 76%) of 4-nitro-N-(tert-octyl)benzamide are obtained in the form of an off-white powder which is used as is in the following stage.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08323624B2 |
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| Source dataset | uspto-grants-2012_12 |
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| ORD ID | ord-dcaee025a52d4eec942964c83baccecf |
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| Source note | uspto-grants-2012_12 |
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