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Propanoic acid, 3-((2-methoxy-2-oxoethyl)thio)-, methyl ester → 2-Thiophenecarboxylic acid, tetrahydro-3-oxo-, methyl ester

HRID 595057
ノート
印刷プレビュー

反応式

HRID 595057 の反応式
[Li].[CH3:2][O:3][C:4](=[O:13])[CH2:5][S:6][CH2:7][CH2:8][C:9](OC)=[O:10]>CO>[O:10]=[C:9]1[CH2:8][CH2:7][S:6][CH:5]1[C:4]([O:3][CH3:2])=[O:13]
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 2

HCID 81891Propanoic acid, 3-((2-methoxy-2-oxoethyl)thio)-, methyl esterHCID 3028194Lithium

生成物 1

HCID 1028702-Thiophenecarboxylic acid, tetrahydro-3-oxo-, methyl ester収率 43.2%

試薬・触媒・溶媒 1

HCID 887Methanol溶媒

実験手順

Lithium metal (2.70 g, 390.15 mmol) was added to 500 mL of methanol in an ice-bath. Then at rt methyl 3-(2-methoxy-2-oxoethylthio)propanoate (50.0 g, 260.10 mmol) was added dropwise to the solution. The reaction mixture was stirred overnight. The resulting reaction mixture was evaporated to remove the solvent. The mixture was neutralized to pH=7-8 with 3N HCl and extracted with dichloromethane. The organic layers were combined, washed with brine, dried over anhydrous Na2SO4, filtered and evaporated. The crude residue obtained contained the target as the only isolable product. Purification by column chromatography on silica gel (eluent: PE/EA=20/1-5/1) provided methyl 3-oxo-tetrahydrothiophene-2-carboxylate as a colourless oil (18.0 g, 43%).

後処理

  1. customThe resulting reaction mixture
  2. customwas evaporated
  3. customto remove the solvent
  4. extractionextracted with dichloromethane
  5. washwashed with brine
  6. dry with materialdried over anhydrous Na2SO4
  7. filtrationfiltered
  8. customevaporated
  9. customThe crude residue obtained
  10. customPurification by column chromatography on silica gel (eluent: PE/EA=20/1-5/1)

出典と根拠

ORDレコード
ord-35bde052d3db4030a1b345e35d1e13d9
出典データセット
uspto-grants-2016_01
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US09242993B2

反応ノート

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