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Acetic Acid → HCID 12710774、化合物

HRID 595062
ノート
印刷プレビュー

反応式

HRID 595062 の反応式
C[O-].[Na+].C[O:5][C:6](=O)[CH2:7][S:8][CH:9]([CH3:15])[CH2:10][C:11]([O:13][CH3:14])=[O:12].C(O)(=O)C.C([O-])([O-])=O.[Na+].[Na+]>C1(C)C=CC=CC=1>[CH3:15][CH:9]1[CH:10]([C:11]([O:13][CH3:14])=[O:12])[C:6](=[O:5])[CH2:7][S:8]1
参加物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 176Acetic AcidHCID 10340Sodium CarbonateHCID 2777633Methyl 3-[(2-methoxy-2-oxoethyl)thio]butanoateHCID 10942334Sodium Methoxide

生成物 1

HCID 12710774HCID 12710774、化合物収率 32%

試薬・触媒・溶媒 1

HCID 1140Toluene溶媒

実験手順

To a suspension of sodium methoxide (5.89 g, 109.2 mmol) in toluene (150 mL) was added methyl 3-(2-methoxy-2-oxoethylthio)butanoate (150 g, 72.8 mmol) dropwise. The resultant mixture was heated to reflux and stirred overnight. The resulting reaction mixture was cooled then poured into a mixture of 10.0 mL of acetic acid in 150.0 g of crushed ice. The solution was made basic (pH=8-9) by addition of saturated Na2CO3 and the resulting mixture extracted with ethyl acetate. The combined organic layers were then combined and washed with brine, dried over anhydrous Na2SO4, filtered, evaporated, and the residue purified by column chromatography (eluent: petroleum ether/ethyl acetate=20/1-5/1) to provide methyl 2-methyl-4-oxo-tetrahydrothiophene-3-carboxylate as a colorless oil (4.0 g, 32%).

後処理

  1. temperatureto reflux
  2. customThe resulting reaction mixture
  3. temperaturewas cooled
  4. extractionthe resulting mixture extracted with ethyl acetate
  5. washwashed with brine
  6. dry with materialdried over anhydrous Na2SO4
  7. filtrationfiltered
  8. customevaporated
  9. customthe residue purified by column chromatography (eluent: petroleum ether/ethyl acetate=20/1-5/1)

出典と根拠

ORDレコード
ord-3fc09a8f3a8f434aa5f928cc82a8432e
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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