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Ethyl bromoacetate → (1,3-benzodioxol-5-yloxy)acetic acid

HRID 1767413
ノート
印刷プレビュー

反応式

HRID 1767413 の反応式
[CH2:1]1[O:5][C:4]2[CH:6]=[C:7]([OH:10])[CH:8]=[CH:9][C:3]=2[O:2]1.C(=O)([O-])[O-].[K+].[K+].Br[CH2:18][C:19]([O:21]CC)=[O:20]>CC(C)=O>[CH2:1]1[O:2][C:3]2[CH:9]=[CH:8][C:7]([O:10][CH2:18][C:19]([OH:21])=[O:20])=[CH:6][C:4]=2[O:5]1
参加物実験手順後処理出典と根拠反応ノート

参加物

5

反応物 3

HCID 7748Ethyl bromoacetateHCID 11430Potassium CarbonateHCID 68289Sesamol

生成物 1

HCID 1531512(1,3-benzodioxol-5-yloxy)acetic acid収率 11.5%

試薬・触媒・溶媒 1

HCID 180Acetone溶媒

実験手順

The mixture of sesamol (270 mg, 2.0 mmol), potassium carbonate (910 mg, 6.6 mmol), ethyl bromoacetate (2.55 ml, 22.9 mmol) and acetone (25 ml) was refluxed for 21 h. After cooling, the mixture was filtered to remove potassium carbonate. The filtrate was concentrated under reduced pressure. To this residue, 20 ml dioxane and 14 ml 5% sodium hydroxide solution were added. After the uiixture was stirred at room temperature overnight, it was acidified with concentrated hydrochloric acid to pH 2, and then extracted three times with ethyl acetate (20 ml each). Organic phases were combined, washed with water and brine, dried over magnesium sulfate, filtered, and then evaporated in vacuo. The residue was recrystallized from chloroform and acetone to give 45 mg 3,4-methylenedioxyphenoxyacetic acid as white crystals, mp 149-151° C.

後処理

  1. temperaturewas refluxed for 21 h
  2. temperatureAfter cooling
  3. filtrationthe mixture was filtered
  4. customto remove potassium carbonate
  5. concentrationThe filtrate was concentrated under reduced pressure
  6. additionTo this residue, 20 ml dioxane and 14 ml 5% sodium hydroxide solution were added
  7. extractionextracted three times with ethyl acetate (20 ml each)
  8. washwashed with water and brine
  9. dry with materialdried over magnesium sulfate
  10. filtrationfiltered
  11. customevaporated in vacuo
  12. customThe residue was recrystallized from chloroform and acetone

出典と根拠

ORDレコード
ord-32ae8cf0e49b4c8786aa1717997b02a3
出典データセット
uspto-grants-2007_06
DOI
10.6084/m9.figshare.5104873.v1
特許番号
USRE039707E1

反応ノート

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