Hydrochloric Acid → 1-Iodo-2-methyl-3-(trifluoromethyl)benzene

HRID 1670775ノート

反応式

HRID 1670775 の反応式
N[C:2]1[C:3]([CH3:12])=[C:4]([C:8]([F:11])([F:10])[F:9])[CH:5]=[CH:6][CH:7]=1.Cl.N([O-])=O.[Na+].[I-:18].[K+].[OH-].[Na+]>O>[I:18][C:2]1[C:3]([CH3:12])=[C:4]([C:8]([F:11])([F:10])[F:9])[CH:5]=[CH:6][CH:7]=1

参加物

7

反応条件

温度
0 °C

実験手順

3-Amino-2-methylbenzotrifluoride (Aldrich Co., 5.25 g) was added to a mixture of concentrated hydrochloric acid (20 ml) and water (20 ml) and, under ice-cooling, sodium nitrite (3.31 g) dissolved in water (10 ml) was added dropwise thereto. The mixture was stirred at 0° C. for 1 hr. Potassium iodide (9.95 g) dissolved in water (20 ml) was added to the reaction mixture. The mixture was stirred at −4° C. for 2 hr. The mixture was adjusted to pH 11 or above with a 6N aqueous sodium hydroxide solution, and an aqueous thiosodium sulfate solution was added thereto. The mixture was extracted with ethyl acetate. The extract was washed with saturated brine and dried. The solvent was evaporated under reduced pressure to give a brown oil. The oil was purified by silica gel column chromatography (elution solvent: hexane) to give 3-iodo-2-methylbenzotrifluoride (6.28 g, yield 73%).

後処理

  1. temperaturecooling
  2. additionwas added dropwise
  3. additionwas added to the reaction mixture
  4. stirringThe mixture was stirred at −4° C. for 2 hr
  5. extractionThe mixture was extracted with ethyl acetate
  6. washThe extract was washed with saturated brine
  7. customdried
  8. customThe solvent was evaporated under reduced pressure
  9. customto give a brown oil
  10. customThe oil was purified by silica gel column chromatography (elution solvent: hexane)

出典と根拠

ORDレコード
ord-c61fc30ada0e4d4da524b8fd642907b4
出典データセット
uspto-grants-2011_08
特許番号
US07994196B2

反応ノート

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