Methyl iodide → 3-Chloro-5-fluoro-2-methoxybenzaldehyde

HRID 647202ノート

反応式

HRID 647202 の反応式
[Cl:1][C:2]1[C:3]([OH:11])=[C:4]([CH:7]=[C:8]([F:10])[CH:9]=1)[CH:5]=[O:6].[C:12](=O)([O-])[O-].[K+].[K+].CI>CC(C)=O>[Cl:1][C:2]1[C:3]([O:11][CH3:12])=[C:4]([CH:7]=[C:8]([F:10])[CH:9]=1)[CH:5]=[O:6]

参加物

5

反応物 3

HCID 6328Methyl iodideHCID 11430Potassium CarbonateHCID 27827493-Chloro-5-fluoro-2-hydroxybenzaldehyde

生成物 1

HCID 130935603-Chloro-5-fluoro-2-methoxybenzaldehyde収率 69.3%

試薬・触媒・溶媒 1

HCID 180Acetone溶媒

実験手順

3-Chloro-5-fluoro-2-hydroxybenzaldehyde (2.5 g., 0.014 mole) was taken into 25 ml. of acetone. Potassium carbonate (2.48 g., 0.018 mole) and methyl iodide (2.55 g., 0.018 mole) were added in sequence and the mixture stirred for 16 hours at room temperature. The reaction mixture was filtered and the filtrate concentrated to an oil. The oil was partitioned between methylene chloride and water. The organic layer was washed in sequence with fresh water, 1 N sodium hydroxide and brine, dried over anhydrous magnesium sulfate, and concentrated to yield 3-chloro-5-fluoro-2-methoxybenzaldehyde (1.83 g., 69%; m.p. 59°-62° C.).

後処理

  1. filtrationThe reaction mixture was filtered
  2. concentrationthe filtrate concentrated to an oil
  3. customThe oil was partitioned between methylene chloride and water
  4. washThe organic layer was washed in sequence with fresh water, 1 N sodium hydroxide and brine
  5. dry with materialdried over anhydrous magnesium sulfate
  6. concentrationconcentrated

出典と根拠

ORDレコード
ord-52d716b966b345be9568d16dfa910c4f
出典データセット
uspto-grants-1983_10
特許番号
US04407811

反応ノート

読み込み中…