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Acetic Acid → 1-(2,4-Dihydroxy-5-isobutyl-phenyl)-ethanone

HRID 1891182
ノート
印刷プレビュー

反応式

HRID 1891182 の反応式
[CH2:1]([C:5]1[CH:10]=[CH:9][C:8]([OH:11])=[CH:7][C:6]=1[OH:12])[CH:2]([CH3:4])[CH3:3].B(F)(F)F.[CH3:17][CH2:18][O:19]CC.C(O)(=O)C.CC([O-])=O.[Na+]>>[OH:11][C:8]1[CH:7]=[C:6]([OH:12])[C:5]([CH2:1][CH:2]([CH3:4])[CH3:3])=[CH:10][C:9]=1[C:18](=[O:19])[CH3:17]
参加物反応条件実験手順後処理出典と根拠反応ノート

参加物

5

反応物 4

HCID 176Acetic AcidHCID 8000Boron trifluoride etherateHCID 517045Sodium AcetateHCID 139510854-Isobutylresorcinol

生成物 1

HCID 592647801-(2,4-Dihydroxy-5-isobutyl-phenyl)-ethanone

反応条件

温度
90 °C

実験手順

4-Isobutyl-benzene-1,3-diol (1 eq) was taken up in BF3.OEt2 (6 eq) and acetic acid (2 eq) was added. The solution was heated for 16 hours at 90° C. than allowed to cool to room temperature. The solution was added drop wise to 10% NaOAc (aq) and allowed to stand for 4 hours, before being extracted twice with diethyl ether. The organic phases were combined and washed with sat. NaHCO3 (aq), then dried over magnesium sulfate, filtered and concentrated in vacuo to give 1-(2,4-dihydroxy-5-isobutyl-phenyl)-ethanone, which was used without additional purification.

後処理

  1. temperatureto cool to room temperature
  2. extractionbefore being extracted twice with diethyl ether
  3. washwashed with sat. NaHCO3 (aq)
  4. dry with materialdried over magnesium sulfate
  5. filtrationfiltered
  6. concentrationconcentrated in vacuo

出典と根拠

ORDレコード
ord-db4a9c568f8f4b1e9f8133dc075f8499
出典データセット
uspto-grants-2013_08
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US08507480B2

反応ノート

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このページの内容参加物反応条件実験手順後処理出典と根拠反応ノート