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Trifluoroacetic acid → 3-[(2-Methoxy-2-oxoethyl)thio]butanoic acid

HRID 1360178
ノート
印刷プレビュー

反応式

HRID 1360178 の反応式
[CH3:1][O:2][C:3](=[O:16])[CH2:4][S:5][CH:6]([CH3:15])[CH2:7][C:8]([O:10]C(C)(C)C)=[O:9].FC(F)(F)C(O)=O>ClCCl>[CH3:1][O:2][C:3](=[O:16])[CH2:4][S:5][CH:6]([CH3:15])[CH2:7][C:8]([OH:10])=[O:9]
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 6422Trifluoroacetic acidHCID 86621910t-Butyl 3-[(2-methoxy-2-oxoethyl)thio]butanoate2 回

生成物 1

HCID 436178343-[(2-Methoxy-2-oxoethyl)thio]butanoic acid収率 85%

試薬・触媒・溶媒 1

HCID 6344Dichloromethane溶媒

実験手順

1.5 g (6.0 mmol) of t-butyl 3-[(2-methoxy-2-oxoethyl)thio]butanoate (product of step 1) was stirred at room temperature with 10 mL of dichloromethane and 5 mL of trifluoroacetic acid for 6 hours, followed by distillation under reduced pressure. After addition of 40 mL of ethylacetoacetate 40 mL and washing with water, an organic layer was dried over anhydrous magnesium sulfate. The solvent was distilled off under reduced pressure and then the residue was purified by column chromatography to give 1 g (5.1 mmol) of the title compound in a yield of 85%.

後処理

  1. distillationfollowed by distillation under reduced pressure
  2. additionAfter addition of 40 mL of ethylacetoacetate 40 mL
  3. washwashing with water
  4. dry with materialan organic layer was dried over anhydrous magnesium sulfate
  5. distillationThe solvent was distilled off under reduced pressure
  6. customthe residue was purified by column chromatography

出典と根拠

ORDレコード
ord-b8086375fb1449a4bfb1e2a03d80a367
出典データセット
uspto-grants-2011_02
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US07879848B2

反応ノート

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このページの内容参加物実験手順後処理出典と根拠反応ノート