HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 877132Generated: October 30, 2026
1,2-Ethanediamine, N1,N1,N2-trimethyl- → HCID 86698330, compound
https://huagongshe.com/reaction/877132
Participants
| Role | Name | HCID | Charge |
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| Reactant | 1,2-Ethanediamine, N1,N1,N2-trimethyl- | HCID 67338 | — |
| Reactant | 1,3-Dibromo-5-fluorobenzene | HCID 137003 | — |
| Reactant | HCID 178418922 | HCID 178418922 | — |
| Solvent | Toluene | HCID 1140 | — |
| Product | HCID 86698330 | HCID 86698330 | 24.8% |
Reaction Steps
To a solution of 1,3-dibromo-5-fluorobenzene (LXXIV) (4 g, 15.75 mmol) in toluene (50 mL) was added tBuOK (5.3 g, 47.25 mmol) and N1,N1,N2-trimethylethane-1,2-diamine (2.778 mL, 31.5 mmol). The reaction was stirred at 110° C. overnight. The solvent was removed under vacuum and the residue was partitioned between EtOAc and water. The organic layer was separated, washed with water, brine, dried over MgSO4 and evaporated under vacuum. The crude product was purified on a silica gel column (100% CHCl3→5:95 MeOH:CHCl3) to produce N1-(3-bromo-5-fluorophenyl)-N2,N2-dimethylethane-1,2-diamine (LXXV) as a brown viscous oil (1.02 g, 3.91 mmol, 24.8% yield). 1H NMR (DMSO-d6, 500 MHz) δ ppm 2.17 (s, 6H), 2.40 (t, J=3.5 Hz, 2H), 3.01-3.09 (m, 2H), 6.10 (t, J=5 Hz, 1H), 6.38 (dt, J=12 Hz, J=2 Hz, 1H), 6.51 (dt, J=8.5 Hz, J=2 Hz, 1H), 6.60 (s, 1H); ESIMS found C12H16BrFN2 m/z 261 (M+H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08987298B2 |
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| Source dataset | uspto-grants-2015_03 |
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| ORD ID | ord-3e28c6a4c8d24e33b8048fb84cac3c56 |
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| Source note | uspto-grants-2015_03 |
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