HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1935445Generated: October 25, 2026
5-Chloro-2-methylbenzonitrile → 5-Chloro-2-methylbenzylamine
https://huagongshe.com/reaction/1935445
Participants
| Role | Name | HCID | Charge |
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| Reactant | 5-Chloro-2-methylbenzonitrile | HCID 142743 | — |
| Reactant | Aluminium lithium hydride | HCID 21226445 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 5-Chloro-2-methylbenzylamine | HCID 2757673 | — |
Reaction Steps
A solution of 2-methyl-5-chlorobenzonitrile (2 g, 13.2 mmol), in THF (30 mL) was cooled to −15° C. and treated with 1 M lithium aluminum hydride in THF (13.4 mL). The reaction mixture was allowed to warm gradually to 0° C. over 2 h and was then stirred at room temperature for 1.5 h. It was then cooled to 0° C. and quenched sequentially with EtOAc (1 mL), water (0,5 mL), 15% NaOH (0.5 mL), and water (1.5 mL). After stirring for 1 h, the solids were removed via filtration. The filtrate was concentrated and the resulting residue purified by flash chromatography (98:2 methylene chloride/methanol) to give the product as an oil: 1H NMR (CDCl3) δ7.33 (d, J=2.0 Hz, 1H), 7.08 (m, 2H),, 3.83 (s, 2H),, 2.28 (s, 3H), 1.42 (br s, 2H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06387911B1 |
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| Source dataset | uspto-grants-2002_05 |
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| ORD ID | ord-f4ae60e675734602a9c9c7704f2be6a1 |
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| Source note | uspto-grants-2002_05 |
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