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

HRID 2407421ノート

反応式

HRID 2407421 の反応式
[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

参加物

6

反応条件

温度
-78 °C

実験手順

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) 5 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).

後処理

  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%)

出典と根拠

ORDレコード
ord-970d0a8fe0f94e45b9bb37f087886743
出典データセット
uspto-grants-2014_08
特許番号
US08809545B2

反応ノート

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