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Acetic Anhydride → (E,E)-1-acetoxy-4-ethyl-2,4-heptadiene

HRID 2295016
ノート
印刷プレビュー

反応式

HRID 2295016 の反応式
[CH2:1](/[C:3](=[CH:8]\[CH2:9][CH3:10])/[CH:4]=[CH:5]/[CH2:6][OH:7])[CH3:2].[C:11](OC(=O)C)(=[O:13])[CH3:12]>N1C=CC=CC=1>[C:11]([O:7][CH2:6]/[CH:5]=[CH:4]/[C:3](/[CH2:1][CH3:2])=[CH:8]/[CH2:9][CH3:10])(=[O:13])[CH3:12]
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 7918Acetic AnhydrideHCID 86749298(E,E)-4-ethyl-2,4-heptadien-1-ol

生成物 1

HCID 86749299(E,E)-1-acetoxy-4-ethyl-2,4-heptadiene収率 74.3%

試薬・触媒・溶媒 1

HCID 1049Pyridine溶媒

実験手順

To a solution of (E,E)-4-ethyl-2,4-heptadien-1-ol (10.1 g) in pyridine (29 g) at 0° C. was added dropwise acetic anhydride (22.2 g). After two hours at room temperature, the reaction mixture was evaporated in vacuo. The residue was diluted with ethyl acetate, washed with 0.5N hydrochloric acid and brine, dried over anhydrous magnesium sulfate, and evaporated in vacuo. The residue was chromatographed on silica gel (5% ethyl acetate in hexane) to give (E,E)-1-acetoxy-4-ethyl-2,4-heptadiene (9.75 g) as an oil.

後処理

  1. customthe reaction mixture was evaporated in vacuo
  2. additionThe residue was diluted with ethyl acetate
  3. washwashed with 0.5N hydrochloric acid and brine
  4. dry with materialdried over anhydrous magnesium sulfate
  5. customevaporated in vacuo
  6. customThe residue was chromatographed on silica gel (5% ethyl acetate in hexane)

出典と根拠

ORDレコード
ord-442d74d91b0346fcb231f3e075946fd2
出典データセット
uspto-grants-1997_11
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US05691366

反応ノート

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