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Methanol → Methyl thiophen-2-acetate

HRID 523134
ノート
印刷プレビュー

反応式

HRID 523134 の反応式
[S:1]1[CH:5]=[CH:4][CH:3]=[C:2]1[CH2:6][C:7]([OH:9])=[O:8].OS(O)(=O)=O.[CH3:15]O>>[S:1]1[CH:5]=[CH:4][CH:3]=[C:2]1[CH2:6][C:7]([O:9][CH3:15])=[O:8]
参加物実験手順後処理出典と根拠反応ノート

参加物

4

反応物 3

HCID 887MethanolHCID 1118Sulfuric AcidHCID 159702-Thiopheneacetic acid

生成物 1

HCID 88055Methyl thiophen-2-acetate収率 91%

実験手順

Thiophene acetic acid (27.3 g, 192 mmol) was treated with a solution of H2SO4 (5.76 mL, 108 mmol) in MeOH (384 mL) at reflux for one hour. The reaction was then cooled to room temperature, concentrated by rotovap, diluted with ether, washed with 5% sodium bicarbonate and brine. The organic phase was then dried with magnesium sulfate and concentrated by rotovap to yield the product as a yellow oil (27.4 g, 176 mmol, 91%), which was used without further purification. The product matches data for commercially available methyl 2-(thiophen-2-yl)acetate (CAS No. 19432-68-9).

後処理

  1. temperatureat reflux for one hour
  2. concentrationconcentrated by rotovap
  3. additiondiluted with ether
  4. washwashed with 5% sodium bicarbonate and brine
  5. dry with materialThe organic phase was then dried with magnesium sulfate
  6. concentrationconcentrated by rotovap

出典と根拠

ORDレコード
ord-a124dfd8d8a5438aaaece588359dfdb7
出典データセット
uspto-grants-2016_05
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US09334304B2

反応ノート

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