HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 403091Generated: October 30, 2026
Triethylamine → 4-Nitro-N-(tert-octyl)benzamide
https://huagongshe.com/reaction/403091
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | 4-Nitrobenzoyl chloride | HCID 8502 | — |
| Reactant | tert-Octylamine | HCID 61017 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | 4-Nitro-N-(tert-octyl)benzamide | HCID 698029 | 76% |
Reaction Steps
Tert-octylamine (51.7 g, 0.4 mol) and triethylamine (61.2 ml, 0.44 mol) in 260 ml of dichloromethane were introduced into a reactor. It was heated to 70° C. then 4-nitrobenzoyl chloride (77.9 g, 0.42 mol) was added in small portions over 50 minutes. It was heated under reflux for 4 hours. The reaction mixture was poured over ice water; it was extracted with dichloromethane, dried and the solvent was evaporated off. The beige precipitate obtained was 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 were obtained in the form of an off-white powder and used as is in the next step.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08747816B2 |
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| Source dataset | uspto-grants-2014_06 |
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| ORD ID | ord-f0eabef875d849798a1fa6e4fe0edf0f |
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| Source note | uspto-grants-2014_06 |
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