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(+/-)-3-[2,4-Bis(methoxymethoxy)phenyl]cyclohexanone → (+/-)-3-(2,4-Dihydroxyphenyl)cyclohexanone

HRID 2307152
ノート
印刷プレビュー

反応式

HRID 2307152 の反応式
COC[O:4][C:5]1[CH:10]=[C:9]([O:11]COC)[CH:8]=[CH:7][C:6]=1[CH:15]1[CH2:20][CH2:19][CH2:18][C:17](=[O:21])[CH2:16]1>CO>[OH:4][C:5]1[CH:10]=[C:9]([OH:11])[CH:8]=[CH:7][C:6]=1[CH:15]1[CH2:20][CH2:19][CH2:18][C:17](=[O:21])[CH2:16]1
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

3

反応物 1

HCID 22337753(+/-)-3-[2,4-Bis(methoxymethoxy)phenyl]cyclohexanone

生成物 1

HCID 12788196(+/-)-3-(2,4-Dihydroxyphenyl)cyclohexanone

試薬・触媒・溶媒 1

HCID 887Methanol溶媒

反応条件

温度
50 °C

実験手順

(±)-3-[2,4-Bis(methoxymethoxy)phenyl]cyclohexanone (35 mg) in methanol (4 ml) containing acidic ion exchange resin (300 mg) was stirred at 50° C. for 6 hr, and then at ambient temperature for 16 hr. The mixture was evaporated in vacuo and the residue was redissolved in acetone (4 ml) containing water (2 drops) and stirred at 50° C. for 8 hr, then at ambient temperature for 64 hr. The mixture was filtered through celite and purified by flash column chromatography (SiO2, petroleum ether/ethyl acetate 1:1 v/v) to furnish the title compound as a white solid containing an equilibrium mixture of cyclized and uncyclized forms (31 mg, 76%). δH (DMSO) 1.1-2.3 (8H, overlapping m), 3.0 (1H, m), 6.08 (0.5H, bs), 6.16 (1H, bd), 6.25 (0.5H, bs), 6.53 (0.5H, bs), 6.75 (0.5H, d), 6.89 (0.5H, b), 8.98 (0.5H, bs), 9.02 (0.5H, bs), 9.17 (0.5H, bs); m/z (ES−) 205 (M−H)−.

後処理

  1. waitat ambient temperature for 16 hr
  2. customThe mixture was evaporated in vacuo
  3. dissolutionthe residue was redissolved in acetone (4 ml)
  4. additioncontaining water (2 drops)
  5. stirringstirred at 50° C. for 8 hr
  6. waitat ambient temperature for 64 hr
  7. filtrationThe mixture was filtered through celite
  8. custompurified by flash column chromatography (SiO2, petroleum ether/ethyl acetate 1:1 v/v)

出典と根拠

ORDレコード
ord-04d2488cf4c44f6e93e22eef9456679f
出典データセット
uspto-grants-2004_12
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US06828460B2

反応ノート

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