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Dimethylformamide → Benzeneacetic acid, 4-(dodecyloxy)-

HRID 2165333
ノート
印刷プレビュー

反応式

HRID 2165333 の反応式
[CH3:1]N(C)C=O.CC[C:8]1[CH:13]=[C:12](O)[CH:11]=[CH:10][C:9]=1[O:15][C:16]([CH3:18])=O.C(Br)C[CH2:21][CH2:22][CH2:23][CH2:24][CH2:25][CH2:26][CH2:27][CH2:28][CH2:29][CH3:30].[C:32](=[O:35])([O-])[O-:33].[K+].[K+]>O>[CH2:16]([O:15][C:9]1[CH:8]=[CH:13][C:12]([CH2:1][C:32]([OH:33])=[O:35])=[CH:11][CH:10]=1)[CH2:18][CH2:30][CH2:29][CH2:28][CH2:27][CH2:26][CH2:25][CH2:24][CH2:23][CH2:22][CH3:21]
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

6

反応物 4

HCID 6228DimethylformamideHCID 89191-BromododecaneHCID 11430Potassium CarbonateHCID 46173007HCID 46173007、化合物

生成物 1

HCID 10336152Benzeneacetic acid, 4-(dodecyloxy)-収率 63%

試薬・触媒・溶媒 1

HCID 962Water溶媒

反応条件

温度
100 °C

実験手順

To a dimethylformamide (DMF, 100 ml) solution of ethyl 4-hydroxyphenyl acetate (18 g, 0.1 mol.) and dodecyl bromide (25 g, 0.1 mol.) was added potassium carbonate (15 g, 0.1 mol.). The mixture was stirred at 100° C. for one hour. To the reaction solution, after cooling, was added water (200 ml), which was subjected to extraction with isopropyl ether (IPE). The organic layer was washed with water, dried and concentrated under reduced pressure. The concentrate was dissolved in a mixture of methanol (100 ml) and tetrahydrofuran (THF, 100 ml). To the solution was added aqueous sodium hydroxide (10 g, 0.25 xol.), and the mixture was stirred at 50° C. The reaction solution was concentrated under reduced pressure, and the pH was adjusted to 4, followed by extraction with ethyl acetate. The organic layer was washed with water, dried and concentrated under reduced pressure to leave crude crystals Recrystallization from hexane-IPE gave 4-dodecyloxyphenylacetic acid (1-e, 20 g, 63%).

後処理

  1. temperatureTo the reaction solution, after cooling
  2. extractionwas subjected to extraction with isopropyl ether (IPE)
  3. washThe organic layer was washed with water
  4. customdried
  5. concentrationconcentrated under reduced pressure
  6. dissolutionThe concentrate was dissolved in a mixture of methanol (100 ml) and tetrahydrofuran (THF, 100 ml)
  7. additionTo the solution was added aqueous sodium hydroxide (10 g, 0.25 xol.)
  8. stirringthe mixture was stirred at 50° C
  9. concentrationThe reaction solution was concentrated under reduced pressure
  10. extractionfollowed by extraction with ethyl acetate
  11. washThe organic layer was washed with water
  12. customdried
  13. concentrationconcentrated under reduced pressure
  14. customto leave crude
  15. customcrystals Recrystallization from hexane-IPE

出典と根拠

ORDレコード
ord-558d21888ece4ddfa2b6bc46ff6f12ce
出典データセット
uspto-grants-1990_07
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US04939274

反応ノート

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