HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1844630Generated: November 1, 2026
4-Bromo-3-methylbenzonitrile → (4-Bromo-3-methylphenyl)methanamine
https://huagongshe.com/reaction/1844630
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 4-Bromo-3-methylbenzonitrile | HCID 2737494 | — |
| Reactant | Aluminium lithium hydride | HCID 21226445 | — |
| Solvent | Diethyl Ether | HCID 3283 | — |
| Product | (4-Bromo-3-methylphenyl)methanamine | HCID 21756143 | — |
Reaction Steps
To a solution of 4-bromo-3-methyl-benzonitrile (commercially available) (15 g) in diethyl ether (150 ml) under an argon atmosphere was added a solution of lithium aluminum hydride in diethyl ether (1M) (150 ml) at ambient temperature. The reaction mixture was stirred at 40° C. for 2 hours. Then the reaction mixture was cooled to 0° C. and quenched by successive addition of water (10.5 ml), aqueous sodium hydroxide (20% w/w) (7.5 ml) and water (37.5 ml). The phases were separated. The organic phase was filtered through a plug of silica gel and the filtrate concentrated to give 4-bromo-3-methyl-benzylamine (15.11 g) as a yellow oil. 1H-NMR (400 MHz, CDCl3): 7.47 (d, 1H), 7.19 (s, 1H), 6.98 (d, 1H), 3.80 (s, 2H), 2.39 (s, 3H) ppm.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08946447B2 |
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| Source dataset | uspto-grants-2015_02 |
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| ORD ID | ord-f0e879722bce4b1d8b0e208851969172 |
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| Source note | uspto-grants-2015_02 |
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