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Formaldehyde → Benzenemethanol, 2-hydroxy-3-methoxy-5-(2-propenyl)-

HRID 2382502
ノート
印刷プレビュー

反応式

HRID 2382502 の反応式
[C:1]1([O:11][CH3:12])[C:2](=[CH:4][CH:5]=[C:6]([CH:10]=1)[CH2:7][CH:8]=[CH2:9])[OH:3].[OH-].[Na+].C=O.[C:17](OCC)(=[O:19])C>O>[CH2:7]([C:6]1[CH:10]=[C:1]([O:11][CH3:12])[C:2]([OH:3])=[C:4]([CH2:17][OH:19])[CH:5]=1)[CH:8]=[CH2:9]
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 712FormaldehydeHCID 3314EugenolHCID 8857Ethyl AcetateHCID 14798Sodium Hydroxide

生成物 1

HCID 10867203Benzenemethanol, 2-hydroxy-3-methoxy-5-(2-propenyl)-

試薬・触媒・溶媒 1

HCID 962Water溶媒2 回

実験手順

In a 2 liter round bottom flask equipped with nitrogen inlet and magnetic stirrer was dissolved eugenol, 99% (Alfa Aesar) in a solution comprised of 286 g NaOH in 1.2 L water at 0° C. A solution of formaldehyde (828 g, 10.2 mol), 37 wt. % solution in water, A.C.S. reagent (Sigma-Aldrich) was added dropwise to the stirring solution. The mixture was stirred under nitrogen at ambient temperature for 4 hours and then 55° C. for 20 h. The reaction mixture was poured into 1 L ethyl acetate and washed with 1 N HCl and deionized water. The crude product containing ˜30 mol % unreacted eugenol was used in the next step without further purification.

後処理

  1. customIn a 2 liter round bottom flask equipped with nitrogen inlet and magnetic stirrer
  2. additionreagent (Sigma-Aldrich) was added dropwise to the stirring solution
  3. wait55° C. for 20 h
  4. washwashed with 1 N HCl
  5. additionThe crude product containing ˜30 mol % unreacted eugenol
  6. customwas used in the next step without further purification

出典と根拠

ORDレコード
ord-1caa673c6a0943a185a9d18cf25b9100
出典データセット
uspto-grants-2012_09
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US08262947B2

反応ノート

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