HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 876197Generated: October 30, 2026
Hydrochloric Acid → 1-Amino-4(1,8-nonadiene-5-yloxy)benzene
https://huagongshe.com/reaction/876197
Participants
| Role | Name | HCID | Charge |
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| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | 1-Nitro-4-(1,8-nonadiene-5-yloxy)benzene | HCID 86708878 | — |
| Catalyst | Iron | HCID 23925 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | 1-Amino-4(1,8-nonadiene-5-yloxy)benzene | HCID 86708879 | 688.6% |
Reaction Steps
A 300 ml-capacity three neck flask containing a stirring bar and connected to a condenser was sufficiently dried. Then, a nitrogen atmosphere was established in the flask. 1-nitro-4-(1,8-nonadiene-5-yloxy)benzene (11) (4.01 g, 1.4 mmol), an iron powder (3.13 g, 5.6 mmol), and ethanol (50%, 10 ml) were introduced into the flask, and the mixture thus obtained was started to be stirred while heating the flask in an oil bath. Further, HCl (0.52 ml) and ethanol (50%, 2.5 ml) were slowly added to the mixture, which was then stirred for 2 hours. Thereafter, an aqueous sodium hydroxide solution was added to the mixture to stop the reaction, and an organic layer was extracted with ethyl acetate. This organic layer was dried over Na2SO4 and filtered, a solvent was distilled of under reduced pressure, and the organic layer was purified by flash chromatography on silica gel (hexane:ethyl acetate=10:1). Thus, 1-amino-4(1,8-nonadiene-5-yloxy)benzene (12) (2.39 g, 9.64×10−3 mol, yield: 69%) was obtained as an intended compound.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08987044B2 |
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| Source dataset | uspto-grants-2015_03 |
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| ORD ID | ord-6eb22a9fa07b4162a0af5932d1b74519 |
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| Source note | uspto-grants-2015_03 |
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