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Ethyl Acetoacetate → Ethyl 3-oxo-5-m-toluylpentanoate

HRID 324420
ノート
印刷プレビュー

反応式

HRID 324420 の反応式
[C:1]([O:7][CH2:8][CH3:9])(=[O:6])[CH2:2][C:3]([CH3:5])=[O:4].C([N-]C(C)C)(C)C.[Li+].[CH3:18][C:19]1[CH:20]=[C:21]([CH:24]=[CH:25][CH:26]=1)[CH2:22]Br>O1CCCC1>[CH3:18][C:19]1[CH:20]=[C:21]([CH2:22][CH2:5][C:3](=[O:4])[CH2:2][C:1]([O:7][CH2:8][CH3:9])=[O:6])[CH:24]=[CH:25][CH:26]=1
参加物実験手順後処理出典と根拠反応ノート

参加物

5

反応物 3

HCID 8868Ethyl AcetoacetateHCID 12099m-Xylyl bromideHCID 2724682Lithium diisopropylamide

生成物 1

HCID 54309110Ethyl 3-oxo-5-m-toluylpentanoate

試薬・触媒・溶媒 1

HCID 8028Tetrahydrofuran溶媒

実験手順

Ethyl acetoacetate (74.5 ml) was added dropwise to a solution of lithium diisopropylamide (2.0M solution in heptane/tetrahydrofuran/ethylbenzene, 600 ml) in tetrahydrofuran (2.5 L) at 0° C. The mixture was stirred for 30 min then 3-methylbenzylbromide (79 ml) was added dropwise. The mixture was stirred for 1 hour at 0° C. then quenched with 2M HCl. The mixture was extracted with ethyl acetate, the extracts washed with water, dried (MgSO4) and evaporated to give an oil which was purified by chromatography eluting with 5-10% ethyl acetate in isohexane.

後処理

  1. stirringThe mixture was stirred for 1 hour at 0° C.
  2. customthen quenched with 2M HCl
  3. extractionThe mixture was extracted with ethyl acetate
  4. washthe extracts washed with water
  5. dry with materialdried (MgSO4)
  6. customevaporated
  7. customto give an oil which
  8. customwas purified by chromatography
  9. washeluting with 5-10% ethyl acetate in isohexane

出典と根拠

ORDレコード
ord-4567031854d64034950188e2e4720135
出典データセット
uspto-grants-2001_04
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US06218376B1

反応ノート

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