HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 986874Generated: October 30, 2026
6-Aminohexanoic Acid → HCID 15992782, compound
https://huagongshe.com/reaction/986874
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 6-Aminohexanoic Acid | HCID 564 | — |
| Reactant | p-Fluoronitrobenzene | HCID 9590 | — |
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | Sodium Bicarbonate | HCID 516892 | — |
| Solvent | Ethanol | HCID 702 | — |
| Solvent | Water | HCID 962 | — |
| Product | HCID 15992782 | HCID 15992782 | 97% |
Reaction Steps
5 g (38.11 mmol) of 6-aminocaproic acid are dissolved in 50 ml of water in the presence of 1.5 g (1 eq) of sodium hydroxide and 4.2 g (1.3 eq) of sodium bicarbonate in a 250 ml three-necked flask equipped with a reflux condenser and a thermometer. A solution of 4.9 ml (1.2 eq) of 4-fluoronitrobenzene in 50 ml of ethanol is run into the mixture, which mixture is subsequently brought to reflux (85°-90° C.) for 48 hours. The mixture is cooled and then extracted 3 times with dichloromethane. The aqueous phase is acidified to pH˜3 with 5N hydrochloric acid. A yellow precipitate is formed; the mixture is left overnight in a refrigerator. The precipitate is pulled dry and washed with water and with acetone. After drying, 9.3 g of a yellow product are obtained, i.e. a final yield of 97%.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06630004B1 |
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| Source dataset | uspto-grants-2003_10 |
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| ORD ID | ord-731370078f1649c8b61fa6fa034e07cf |
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| Source note | uspto-grants-2003_10 |
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