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

HRID 391308ノート

反応式

HRID 391308 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) 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).

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-fa1a219bdb7a468c820c0a6b724c994d
出典データセット
uspto-grants-2013_02
特許番号
US08383827B2

反応ノート

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