HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2296370Generated: October 26, 2026
Hydrochloric Acid → 2-Amino-6-(4-aminophenyl)-6-methylheptane
https://huagongshe.com/reaction/2296370
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Aniline | HCID 6115 | — |
| Reactant | Heptaminol Hydrochloride | HCID 10969 | — |
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Catalyst | Tantalum | HCID 23956 | — |
| Catalyst | Zincchloride | HCID 3007855 | — |
| Solvent | Water | HCID 962 | — |
| Product | 2-Amino-6-(4-aminophenyl)-6-methylheptane | HCID 20156669 | 82% |
Reaction Steps
To a solution of 102 parts of anhydrous zinc chloride in 153 parts of 36% w/w aqueous hydrochloric acid and 200 parts of water are added 140 parts of aniline and 136 parts of 6-hydroxy-6-methyl-2-heptylamine hydrochloride (heptaminol hydrochloride). The whole is charged to a 1 liter tantalum-lined autoclave and stirred at 185° C. for 24 hours. The reaction mixture, after being discharged from the autoclave, is added to a hot solution of 750 parts sodium hydroxide in 1500 parts of water and stirred until cool. The organic phase is extracted with diethylether, washed with water, evaporated and distilled under reduced pressure. After recovering 58 parts of aniline there are obtained 135 parts of 2-amino-6-(4-amino-phenyl)-6-methyl-heptane boiling point 138°-40° C./65 Pa (82% yield based on heptaminol).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04429110 |
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| Source dataset | uspto-grants-1984_01 |
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| ORD ID | ord-3e401ff2a45b426fa5a1c001b420fd1b |
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| Source note | uspto-grants-1984_01 |
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