HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1156561Generated: November 1, 2026
p-Toluenesulfonic acid → HCID 20534900, compound
https://huagongshe.com/reaction/1156561
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | p-Toluenesulfonic acid | HCID 6101 | — |
| Reactant | HCID 12923073 | HCID 12923073 | — |
| Reactant | HCID 20494492 | HCID 20494492 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | HCID 20534900 | HCID 20534900 | — |
Reaction Steps
Isopentylamine was reacted with 4-(4-nitrophenyl)butanoyl chloride to provide N-isopentyl-4-(4-nitrophenyl)butyramide, which when reduced by reaction with diborane afforded N-isopentyl-4-(4-nitrophenyl)butylamine. Reaction of the latter compound with acetyl chloride under the conditions of Example 22 gave N-acetyl-N-isopentyl-4-(4-nitrophenyl)butylamine. Reaction of 21.8 g. of N-acetyl-N-isopentyl-4-(4-nitrophenyl)butylamine with 220 ml. of 1 M diborane in tetrahydrofuran provided, after workup according to the method of Example 22, 19.8 g. of N-ethyl-N-isopentyl-4-(4-nitrophenyl)butylamine. Reaction of the amine with para-toluenesulfonic acid in ethyl acetate afforded N-ethyl-N-isopentyl-4-(4-nitrophenyl)butylaminium tosylate. M.P. 78°-80° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04336269 |
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| Source dataset | uspto-grants-1982_06 |
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| ORD ID | ord-0ae813053bdc40289c10bf79e918844b |
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| Source note | uspto-grants-1982_06 |
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