HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1416537Generated: November 2, 2026
Hydrochloric Acid → 2-(3-Methylbutyl)aniline
https://huagongshe.com/reaction/1416537
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Methanol | HCID 887 | — |
| Reactant | Sodium Bicarbonate | HCID 516892 | — |
| Reactant | 2-(3-Methylbutyl)nitrobenzene | HCID 18417690 | — |
| Solvent | Water | HCID 962 | — |
| Product | 2-(3-Methylbutyl)aniline | HCID 18764094 | 90.9% |
Reaction Steps
To a mixture composed of 10 ml of methanol, 1.3 g (6.4 mmol) of the above 2-(3-methylbutyl)nitrobenzene, and 6.4 ml of concentrated aqueous hydrochloric acid solution, 1.4 g (25.1 mmol) of reduced iron was added in portions and heated to 60° C. with stirring for 1 hour. The reaction mass was poured into water, neutralized with a saturated aqueous sodium hydrogen carbonate solution and filtered to remove precipitated iron hydroxide. The filtrate was extracted with ethyl acetate, washed with a saturated aqueous sodium chloride solution and dried over anhydrous sodium sulfate. The solvent was distilled off under reduced pressure to obtain 0.95 g of the desired product as oil. Yield was 85%.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05914344 |
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| Source dataset | uspto-grants-1999_06 |
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| ORD ID | ord-d793bc36ff3a486a9f8da9f328e57668 |
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| Source note | uspto-grants-1999_06 |
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