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Sodium Iodide → 1-[4-(Methoxymethyl)phenyl]propan-2-one

HRID 434367
ノート
印刷プレビュー

反応式

HRID 434367 の反応式
C1[O:15][C:4]([CH3:14])([CH2:5][C:6]2[CH:11]=[CH:10][C:9]([CH2:12]Br)=[CH:8][CH:7]=2)OC1.[CH3:16][O-:17].[Na+].[I-].[Na+]>CO>[CH3:16][O:17][CH2:12][C:9]1[CH:8]=[CH:7][C:6]([CH2:5][C:4](=[O:15])[CH3:14])=[CH:11][CH:10]=1
参加物実験手順後処理出典と根拠反応ノート

参加物

5

反応物 3

HCID 5238Sodium IodideHCID 10942334Sodium MethoxideHCID 566280772-{[4-(Bromomethyl)phenyl]methyl}-2-methyl-1,3-dioxolane

生成物 1

HCID 204938201-[4-(Methoxymethyl)phenyl]propan-2-one

試薬・触媒・溶媒 1

HCID 887Methanol溶媒3 回

実験手順

1-(4-Bromomethylphenyl)propan-2-one ethylene ketal (1.35 g) in methanol was added to sodium methoxide (from sodium (0.11 g)) in methanol containing a trace of sodium iodide. The mixture was refluxed for 1 hour. Methanol was removed, the residue partitioned between water and ether and the combined organic extracts dried. Removal of the solvent gave an oil which was dissolved in methanol-2 N hydrochloric acid and left for 1 hour at room temperature. Extraction with ether gave the title compound, bp 106°/0.7 mm. τ(CDCl3) 7.9 (3H, s), 7.63 (3H, s), 6.33 (2H, s), 5.54 (2H, s), 2.8 (2H, d, J=8 Hz), 2.6 (2H, d, J=8 Hz).

後処理

  1. temperatureThe mixture was refluxed for 1 hour
  2. customMethanol was removed
  3. customthe residue partitioned between water and ether
  4. customthe combined organic extracts dried
  5. customRemoval of the solvent
  6. customgave an oil which
  7. extractionExtraction with ether

出典と根拠

ORDレコード
ord-0ef15178418849c9ae0a69c2616abdf3
出典データセット
uspto-grants-1983_08
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US04396627

反応ノート

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