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Hydrochloric Acid → (8-Methoxy-2,3-dihydro-1,4-benzodioxin-6-YL)methanol

HRID 2193128
ノート
印刷プレビュー

反応式

HRID 2193128 の反応式
O1CCCC1.[CH3:6][O:7][C:8]1[C:13]2[O:14][CH2:15][CH2:16][O:17][C:12]=2[CH:11]=[C:10]([C:18](OC)=[O:19])[CH:9]=1.[H-].[Al+3].[Li+].[H-].[H-].[H-].Cl>O>[CH3:6][O:7][C:8]1[C:13]2[O:14][CH2:15][CH2:16][O:17][C:12]=2[CH:11]=[C:10]([CH2:18][OH:19])[CH:9]=1
参加物実験手順後処理出典と根拠反応ノート

参加物

6

反応物 4

HCID 313Hydrochloric AcidHCID 8028TetrahydrofuranHCID 18464946Methyl 8-Methoxy-2,3-dihydrobenzo[b][1,4]dioxine-6-carboxylateHCID 21226445Aluminium lithium hydride

生成物 1

HCID 16769335(8-Methoxy-2,3-dihydro-1,4-benzodioxin-6-YL)methanol

試薬・触媒・溶媒 1

HCID 962Water
溶媒

実験手順

To 30 mL of a tetrahydrofuran solution containing 1.06 g of methyl 8-methoxy-2,3-dihydro-1,4-benzodioxin-6-carboxylate, 720 mg of lithium aluminum hydride was added under cooling with ice. The reaction mixture was stirred at room temperature for 1 hour, 5 mL of a 1 mol/L hydrochloric acid and 45 mL of water were added thereto, and the resultant solution was extracted with ethyl acetate. The organic layer was washed with an aqueous saturated sodium chloride solution and dried over anhydrous magnesium sulfate, and the solvent was removed under reduced pressure to obtain 940 mg of a brown oily substance, (8-methoxy-2,3-dihydro-1,4-benzodioxin-6-yl)methanol.

後処理

  1. additionwas added
  2. temperatureunder cooling with ice
  3. extractionthe resultant solution was extracted with ethyl acetate
  4. washThe organic layer was washed with an aqueous saturated sodium chloride solution
  5. dry with materialdried over anhydrous magnesium sulfate
  6. customthe solvent was removed under reduced pressure

出典と根拠

ORDレコード
ord-76315d6cdaa145ca955c4bd5ca3537e0
出典データセット
uspto-grants-2012_12
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US08329694B2

反応ノート

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