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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1183062Generated: November 3, 2026

1,2-Ethanediamine, N1,N1,N2-trimethyl- → HCID 86698330, compound

https://huagongshe.com/reaction/1183062

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1,2-Ethanediamine, N1,N1,N2-trimethyl-HCID 67338—
Reactant1,3-Dibromo-5-fluorobenzeneHCID 137003—
ReactantHCID 178418922HCID 178418922—
SolventTolueneHCID 1140—
ProductHCID 86698330HCID 8669833024.8%

Reaction Conditions

Temperature110 °C

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08664241B2
Source datasetuspto-grants-2014_03
ORD IDord-7bc9253d1da4441eb8dcd32ac8fcdd6d
Source noteuspto-grants-2014_03