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Allyl bromide → HCID 22718066、化合物

HRID 1582795
ノート
印刷プレビュー

反応式

HRID 1582795 の反応式
[CH3:1][O:2][C:3]1[CH:4]=[C:5]2[C:10](=[CH:11][CH:12]=1)[CH:9]=[C:8]([OH:13])[CH:7]=[CH:6]2.C(=O)([O-])[O-].[K+].[K+].[CH2:20](Br)[CH:21]=[CH2:22]>CC(C)=O>[CH3:1][O:2][C:3]1[CH:4]=[C:5]2[C:10](=[CH:11][CH:12]=1)[CH:9]=[C:8]([O:13][CH2:22][CH:21]=[CH2:20])[CH:7]=[CH:6]2
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 7841Allyl bromideHCID 11430Potassium CarbonateHCID 2886346-Methoxy-2-naphthol

生成物 1

HCID 22718066HCID 22718066、化合物収率 91.5%

試薬・触媒・溶媒 1

HCID 180Acetone溶媒

実験手順

6-Methoxy-2-naphthol (22.1 g, 127.0 mmol) was dissolved in acetone (200 ml). Potassium carbonate (70.2 g, 508.0 mmol) and allyl bromide (16.5 ml, 191.0 mmol) were added to the resulting solution followed by stirring for 2 days at room temperature. After the reaction mixture was filtered, the organic solvent was distilled off under reduced pressure. Water was added to the residue, which was then extracted with ethyl acetate. The organic layer was washed with saturated aqueous sodium chloride and dried over anhydrous sodium sulfate. The organic solvent was distilled off again to give 6-methoxy-2-(2-propenyloxy)naphthalene (24.9 g, Yield 91%) as a crude product.

後処理

  1. filtrationAfter the reaction mixture was filtered
  2. distillationthe organic solvent was distilled off under reduced pressure
  3. additionWater was added to the residue, which
  4. extractionwas then extracted with ethyl acetate
  5. washThe organic layer was washed with saturated aqueous sodium chloride
  6. dry with materialdried over anhydrous sodium sulfate
  7. distillationThe organic solvent was distilled off again

出典と根拠

ORDレコード
ord-8fb28a09046f4523b0dbf3a9a915ac8d
出典データセット
uspto-grants-2004_05
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US06737417B2

反応ノート

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