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3-Hydroxybenzaldehyde → Ethyl 2-(3-formylphenoxy)acetate

HRID 619163
ノート
印刷プレビュー

反応式

HRID 619163 の反応式
[OH:1][C:2]1[CH:3]=[C:4]([CH:7]=[CH:8][CH:9]=1)[CH:5]=[O:6].C([O-])([O-])=O.[K+].[K+].Br[CH2:17][C:18]([O:20][CH2:21][CH3:22])=[O:19]>CC(C)=O>[CH2:21]([O:20][C:18]([CH2:17][O:1][C:2]1[CH:3]=[C:4]([CH:7]=[CH:8][CH:9]=1)[CH:5]=[O:6])=[O:19])[CH3:22]
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 1013-HydroxybenzaldehydeHCID 7748Ethyl bromoacetate2 回HCID 11430Potassium Carbonate2 回

生成物 1

HCID 1494377Ethyl 2-(3-formylphenoxy)acetate

試薬・触媒・溶媒 1

HCID 180Acetone溶媒

実験手順

To a mixture of 3-hydroxybenzaldehyde (5.17 g, 42.34 mmol), K2CO3 (5.85 g) and acetone (50 ml) was added ethyl bromoacetate (5.2 ml). The reaction mixture was stirred at room temperature overnight, additional K2CO3 (1 equivalent) was added, the mixture was stirred for one hour, then additional ethyl bromoacetate (0.5 equivalents) was added and the mixture was stirred at room temperature until the reaction was complete. The reaction mixture was filtered, water was added to the filtrate and the solvent was removed. The residue was dissolved in ether, extracted with 1M NaOH (2×100 ml), and the ether layer was dried over MgSO4 and stripped to afford, as a liquid, 7.89 g of 3-(ethoxycarbonylmethoxy)benzaldehyde.

後処理

  1. stirringthe mixture was stirred for one hour
  2. stirringthe mixture was stirred at room temperature until the reaction
  3. filtrationThe reaction mixture was filtered
  4. additionwater was added to the filtrate
  5. customthe solvent was removed
  6. dissolutionThe residue was dissolved in ether
  7. extractionextracted with 1M NaOH (2×100 ml)
  8. dry with materialthe ether layer was dried over MgSO4

出典と根拠

ORDレコード
ord-f5af93014418476a8d8de55d5bfd3c58
出典データセット
uspto-grants-1999_09
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US05958929

反応ノート

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