1,10-Phenanthroline → 252752-46-8
Reaction equation
I[C:2]1[CH:7]=[CH:6][C:5]([CH2:8][C:9]([O:11][CH3:12])=[O:10])=[CH:4][CH:3]=1.C(OC(=O)[NH:22][NH2:23])(OC(C)(C)C)=O.N1C2C(=CC=C3C=2N=CC=C3)C=CC=1.C(=O)([O-])[O-].[Cs+].[Cs+].O1CCOCC1.[ClH:51]>CN(C=O)C.C(OCC)(=O)C.[Cu](I)I.C(OCC)C>[ClH:51].[NH:22]([C:2]1[CH:7]=[CH:6][C:5]([CH2:8][C:9]([O:11][CH3:12])=[O:10])=[CH:4][CH:3]=1)[NH2:23]Participants
Reactant 5
Product 1
Reagents, catalysts & solvents 4
Conditions
- Temperature
- 120 °C
Procedure
A solution of methyl 4-iodophenylacetate (4.25 g, 15.39 mmol) was dissolved in DMF (25 mL). BOC-carbazate (2.44 g, 18.47 mmol), 1,10-phenanthroline (278 mg, 1.54 mmol), copper iodide (147 mg, 0.77 mmol) and cesium carbonate (7.0 g, 21.55 mmol) were added and the mixture heated at 120° C. for 60 min. The reaction mixture was diluted with ethyl acetate (25 mL), washed with water (3×10 mL) and brine (10 mL), dried (MgSO4) and evaporated to leave a brown oil which was purified by flash chromatography on silica gel (elution gradient 0-50% EtOAc in isohexane) to give a colourless oil. The oil was dissolved in 4M HCl Dioxan (20 mL) and stirred at ambient temperature for 3 h giving a thick precipitate. Diethyl ether (100 mL) was added and the precipitate recovered by filtration, washed with ether (2×20 mL) and dried under vacuum to leave methyl 2-(4-hydrazinylphenyl)acetate_hydrochloride as a light brown solid. (1.63 g, 49%)
Workup
- washwashed with water (3×10 mL) and brine (10 mL)
- dry with materialdried (MgSO4)
- customevaporated
- customto leave a brown oil which
- customwas purified by flash chromatography on silica gel (elution gradient 0-50% EtOAc in isohexane)
- customto give a colourless oil
- customgiving a thick precipitate
- filtrationthe precipitate recovered by filtration
- washwashed with ether (2×20 mL)
- customdried under vacuum
Sources & evidence
- ORD record
- ord-d74e86dbaf3a4ff2bfd2d6c5f87fded0
- Source dataset
- uspto-grants-2013_01
- Patent number
- US08344016B2
Reaction notes
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