HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1021399Generated: October 31, 2026
Aluminium lithium hydride → 2-(4-Chloro-2-methylphenyl)ethanamine
https://huagongshe.com/reaction/1021399
Participants
| Role | Name | HCID | Charge |
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| Reactant | Aluminium lithium hydride | HCID 21226445 | — |
| Reactant | 4-Chloro-2-methyl-1-(2-nitrovinyl)benzene | HCID 67025969 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 2-(4-Chloro-2-methylphenyl)ethanamine | HCID 20251955 | 75% |
Reaction Steps
A solution of 4-chloro-2-methyl-1-(2-nitrovinyl)benzene (1.83 g, 9.26 mmol) in tetrahydrofuran (40 mL) was cooled to 0° C. in an ice bath, and a 1M solution of lithium aluminum hydride in tetrahydrofuran (37 mL, 37 mmol) was added, dropwise over 10 minutes. The resulting mixture was stirred in the ice bath for 2 hours 30 minutes, then quenched in the following manner: water (1.5 mL) was added dropwise, and after stirring for 5 minutes, 1M sodium hydroxide (1.5 mL) was added. After stirring for a further 15 minutes, water (5 mL) was added, and the resulting mixture was stirred at ambient temperature for 15 minutes, then filtered through a medium porosity sintered glass funnel. The collected precipitate was washed with ethyl acetate (60 mL). The combined filtrate and wash was dried over sodium sulfate and concentrated to afford 2-(4-chloro-2-methylphenyl)ethanamine as a brown oil (1.17 g, 75% yield).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08716498B2 |
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| Source dataset | uspto-grants-2014_05 |
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| ORD ID | ord-e8de58fce35d489ebbbdb0c661814e62 |
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| Source note | uspto-grants-2014_05 |
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