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Dimethylsulfoxonium methylide → Methyl 2-(4-cyclohexylphenyl)cyclopropanecarboxylate

HRID 446764
ノート
印刷プレビュー

反応式

HRID 446764 の反応式
[CH:1]1([C:7]2[CH:12]=[CH:11][C:10](/[CH:13]=[CH:14]/[C:15]([O:17][CH3:18])=[O:16])=[CH:9][CH:8]=2)[CH2:6][CH2:5][CH2:4][CH2:3][CH2:2]1.[CH3:19]S(C)(=O)=C>CS(C)=O>[CH:1]1([C:7]2[CH:8]=[CH:9][C:10]([CH:13]3[CH2:19][CH:14]3[C:15]([O:17][CH3:18])=[O:16])=[CH:11][CH:12]=2)[CH2:2][CH2:3][CH2:4][CH2:5][CH2:6]1
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 6396768Dimethylsulfoxonium methylideHCID 58358304(E)-methyl 3-(4-cyclohexylphenyl)acrylate

生成物 1

HCID 58358302Methyl 2-(4-cyclohexylphenyl)cyclopropanecarboxylate収率 70.8%

試薬・触媒・溶媒 1

HCID 679Dimethyl Sulfoxide溶媒

実験手順

To a solution of (E)-methyl 3-(4-cyclohexylphenyl)acrylate (200 mg, 0.82 mmol) in DMSO (20 mL) was added freshly prepared Corey's reagent (92 mg, 0.98 mmol) at RT and stirred for 3 h. The reaction was quenched with cold water and then extracted with EtOAc (2×20 mL). The combined organic layers were dried over magnesium sulfate, filtered and then concentrated in vacuo to obtain crude product. The crude material was purified via silica gel column chromatography eluting with 5% EtOAc/95% hexanes to afford methyl 2-(4-cyclohexylphenyl)cyclopropanecarboxylate (150 mg, 47%) as a solid.

後処理

  1. customThe reaction was quenched with cold water
  2. extractionextracted with EtOAc (2×20 mL)
  3. dry with materialThe combined organic layers were dried over magnesium sulfate
  4. filtrationfiltered
  5. concentrationconcentrated in vacuo
  6. customto obtain crude product
  7. customThe crude material was purified via silica gel column chromatography
  8. washeluting with 5% EtOAc/95% hexanes

出典と根拠

ORDレコード
ord-a9adf2ac06774ad5bee9ead93d52c88d
出典データセット
uspto-grants-2013_07
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US08481532B2

反応ノート

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