Iodine → 2-Iodo-1-(methyloxy)-3-{[(methyloxy)methyl]oxy}benzene

HRID 527539ノート

反応式

HRID 527539 の反応式
[CH3:1][O:2][C:3]1[CH:8]=[CH:7][CH:6]=[C:5]([O:9][CH2:10][O:11][CH3:12])[CH:4]=1.[Li]CCCC.[I:18]I>O1CCCC1>[I:18][C:4]1[C:5]([O:9][CH2:10][O:11][CH3:12])=[CH:6][CH:7]=[CH:8][C:3]=1[O:2][CH3:1]

参加物

5

反応条件

温度
-70 °C

実験手順

To a solution of 1-(methyloxy)-3-{[(methyloxy)methyl]oxy}benzene (Intermediate 45, 10 g, 59.5 mmol) in tetrahydrofurane (100 ml, SCRC) precooled to −78° C. was added dropwise BuLi (2.5 M in THF, 28.5 ml, 71.3 mmol, SCRC), maintaining the inner temperature lower than −70° C. After the addition was complete, the mixture was stirred at −70° C. for 2 hours and a solution of iodine (15.09 g, 59.5 mmol, SCRC) in THF (50 ml, SCRC) was added dropwise. The resulting mixture was stirred for 2 hours at room temperature and quenched with a saturated aqueous solution of ammonium chloride (100 ml). The mixture was extracted with ethyl acetate (3 times 300 ml, SCRC) and the combined organic layers were dried, evaporated and purified by silica gel chromatography with as eluents EtOAc:PE (1/100) to afford the title compound (16.2 g) as a yellow liquid.

後処理

  1. customprecooled to −78° C.
  2. additionAfter the addition
  3. stirringThe resulting mixture was stirred for 2 hours at room temperature
  4. customquenched with a saturated aqueous solution of ammonium chloride (100 ml)
  5. extractionThe mixture was extracted with ethyl acetate (3 times 300 ml, SCRC)
  6. customthe combined organic layers were dried
  7. customevaporated
  8. custompurified by silica gel chromatography with as eluents EtOAc

出典と根拠

ORDレコード
ord-b7d7b2c7fe444e0095494a94dc422c8c
出典データセット
uspto-grants-2016_05
特許番号
US09346790B2

反応ノート

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