Water → 6-chloro-2-iodo-1-methyl-1H-benzo[d]imidazole

HRID 1897792Notes

Reaction equation

HRID 1897792 reaction equation
[Cl:1][C:2]1[CH:3]=[CH:4][C:5]2[N:9]=[CH:8][N:7]([CH3:10])[C:6]=2[CH:11]=1.[Li+].CC([N-]C(C)C)C.[I:20]CCI.O>C1COCC1>[Cl:1][C:2]1[CH:3]=[CH:4][C:5]2[N:9]=[C:8]([I:20])[N:7]([CH3:10])[C:6]=2[CH:11]=1

Participants

6

Conditions

Temperature
-78 °C

Procedure

A flask charged with a solution of 6-chloro-1-methyl-1H-benzo[d]imidazole (2 g, 12 mmol) in THF (100 mL) was cooled to −78° C. and 1.8M LDA in THF/hexanes/ethylbenzene (9.34 mL, 16.81 mmol) was added dropwise, and the mixture was stirred at −78° C. for 1 h. A solution of 1,2-diiodoethane (3.72 g, 13.2 mmol) in THF (50 mL) was added dropwise and the mixture was stirred at −78° C. for 1 h. Water (0.3 mL) was added followed by silica gel (20 g) and the mixture was concentrated in vacuo. The residue was purified by silica chromatography eluting with EtOAc in heptane (v/v, 10 to 50%) to give 6-chloro-2-iodo-1-methyl-1H-benzo[d]imidazole. 1H NMR (400 MHz, DMSO-d6) δ ppm 3.76 (s, 3H) 7.19 (dd, J=8.59, 2.02 Hz, 1H) 7.58 (d, J=8.59 Hz, 1H) 7.78 (d, J=2.02 Hz, 1H).

Workup

  1. stirringthe mixture was stirred at −78° C. for 1 h
  2. concentrationthe mixture was concentrated in vacuo
  3. customThe residue was purified by silica chromatography
  4. washeluting with EtOAc in heptane (v/v, 10 to 50%)

Sources & evidence

ORD record
ord-5b8924a20bba439da3d9faf94a322290
Source dataset
uspto-grants-2013_08
Patent number
US08519142B2

Reaction notes

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