2-Chloroethanol → 2-(4-(4-Iodophenyl)piperazin-1-yl)ethanol
Reaction equation
[I:1][C:2]1[CH:7]=[CH:6][C:5]([N:8]2[CH2:13][CH2:12][NH:11][CH2:10][CH2:9]2)=[CH:4][CH:3]=1.CCN(C(C)C)C(C)C.Cl[CH2:24][CH2:25][OH:26]>CC#N.O.C([O-])(O)=O.[Na+]>[I:1][C:2]1[CH:3]=[CH:4][C:5]([N:8]2[CH2:13][CH2:12][N:11]([CH2:24][CH2:25][OH:26])[CH2:10][CH2:9]2)=[CH:6][CH:7]=1Participants
Conditions
- Temperature
- 91 °C
Procedure
To a mixture of 1-(4-iodophenyl)piperazine (2.25 g, 7.8 mmol) and iPr2NEt (3.4 mL, 19.5 mmol, 2.5 equiv.) in CH3CN was added 2-chloroethanol (995 mg, 11.7 mmol, 1.5 equiv.). The resulting mixture was refluxed 7 h (oil temp. 91° C.), then O/N (15 h, oil temp. 83° C.) and 6 h (oil temp. 90° C.) before cooling to rt. After diluting with H2O (30 mL) and sat. NaHCO3 (30 mL), it was extracted with EtOAc (60 mL×2) and washed with H2O and brine. Removal of solvents followed by trituration with MeOH (15 mL) afforded the title compound as a beige solid (1.340 g, 81%). A second trituration of the concentrated mother liquor gave additional 602 mg of crude product as a light brown solid. 1H NMR (400 MHz, DMSO-d6) δ 7.46 (d, J=8.4 Hz, 2H), 6.76 (d, J=8.8 Hz, 2H), 4.43 (t, J=5.0 Hz, 1H), 3.51 (q, J=5.6 Hz, 2H), 3.12-3.07 (m, 4H), 2.55-2.49 (m, 4H, partially overlapping with DMSO signal), 2.41 (t, J=6.0 Hz, 2H); MS ESI 332.9[M+H]+, calcd. for [C12H17IN2O+H]+ 333.0.
Workup
- temperatureO/N (15 h, oil temp. 83° C.) and 6 h (oil temp. 90° C.) before cooling to rt
- extractionwas extracted with EtOAc (60 mL×2)
- washwashed with H2O and brine
- customRemoval of solvents
Sources & evidence
- ORD record
- ord-e5b92ce4bf4442dfb3c671f4a5db4a64
- Source dataset
- uspto-grants-2012_09
- Patent number
- US08263596B2
Reaction notes
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