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Sodium Iodide → 2-Propenoic acid, 3-iodo-, 1-methylethyl ester, (2Z)-

HRID 1465897
ノート
印刷プレビュー

反応式

HRID 1465897 の反応式
[C:1]([O:5][CH:6]([CH3:8])[CH3:7])(=[O:4])[C:2]#[CH:3].[Na+].[I-:10]>CC(O)=O>[I:10]/[CH:3]=[CH:2]\[C:1]([O:5][CH:6]([CH3:8])[CH3:7])=[O:4]
参加物反応条件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 5238Sodium IodideHCID 15626755Propan-2-yl prop-2-ynoate

生成物 1

HCID 585036632-Propenoic acid, 3-iodo-, 1-methylethyl ester, (2Z)-収率 84.1%

試薬・触媒・溶媒 1

HCID 176Acetic Acid溶媒

反応条件

温度
115 °C

実験手順

To a mixture of isopropyl propiolate (350 g, 3.1 moles) in AcOH (1300 mL) was added NaI (930 g, 6.2 moles) at 25° C. The reaction mixture was heated to 115° C. and stirred for 1.5 hrs. The reaction mixture was cooled to 25 to 30° C. and quenched with water followed by extraction with MTBE. The organic layer was washed with saturated bicarbonate, bisulfate and brine solution. The organic layer was dried over sodium sulfate and concentrated under vacuum to give the product (Z)-isopropyl 3-iodoacrylate (626 g; 83.5%). Product was confirmed by 1H NMR.

後処理

  1. temperatureThe reaction mixture was cooled to 25 to 30° C.
  2. customquenched with water
  3. extractionfollowed by extraction with MTBE
  4. washThe organic layer was washed with saturated bicarbonate, bisulfate and brine solution
  5. dry with materialThe organic layer was dried over sodium sulfate
  6. concentrationconcentrated under vacuum

出典と根拠

ORDレコード
ord-45b979ed1b044f5a9dc9bf07ca49108d
出典データセット
uspto-grants-2015_04
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US08999996B2

反応ノート

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このページの内容参加物反応条件実験手順後処理出典と根拠反応ノート