HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1487025Generated: October 26, 2026
Isobutylamine → 2,4-dimethyl-N-(2-methylpropyl)aniline
https://huagongshe.com/reaction/1487025
Participants
| Role | Name | HCID | Charge |
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| Reactant | Isobutylamine | HCID 6558 | — |
| Reactant | Tetrahydrofuran | HCID 8028 | — |
| Reactant | 1-Chloro-2,4-dimethylbenzene | HCID 523153 | — |
| Product | 2,4-dimethyl-N-(2-methylpropyl)aniline | HCID 28422389 | 96.3% |
Reaction Steps
A mixture of 1-chloro-2,4-dimethylbenzene (1687 mg, 12 mmol), isobutylamine (1755 mg, 24.00 mmol), and Caddick catalyst (140 mg, 0.238 mmol) was treated with lithium hexamethyl disilizide in tetrahydrofuran (1 M LHMDS in THF, 15 mL, 15.00 mmol) under nitrogen. The reaction mixture was heated to 70° C. for 45 minutes in a septum-sealed vessel. The cooled mixture was concentrated in vacuo and the residue was partitioned between aqueous citric acid (50 mL) and tert butyl methyl ether (TBME) (2×50 mL). The organic phase was treated with dried MgSO4, the solid removed by filtration and the organic phase was concentrated in vacuo to give (2,4-dimethylphenyl)(2-methylpropyl)amine (2.05 g, 11.56 mmol) as an orange oil. LCMS [LCMS1] Rt 1.03 min, m/z (ES+) 178 (M+H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09428452B2 |
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| Source dataset | uspto-grants-2016_08 |
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| ORD ID | ord-c561e36556e34bc0ab77e7f6e38f36d6 |
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| Source note | uspto-grants-2016_08 |
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