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Sodium Fluoride → HCID 86646135、化合物

HRID 551644
ノート
印刷プレビュー

反応式

HRID 551644 の反応式
[CH:1]([CH:5]([CH2:11][CH:12]=[CH2:13])[C:6](OCC)=[O:7])([CH2:3][CH3:4])[CH3:2].[H-].[Al+3].[Li+].[H-].[H-].[H-].[F-].[Na+]>O1CCCC1.O.C(OCC)(=O)C>[CH:1]([CH:5]([CH2:11][CH:12]=[CH2:13])[CH2:6][OH:7])([CH2:3][CH3:4])[CH3:2]
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

7

反応物 3

HCID 5235Sodium FluorideHCID 21226445Aluminium lithium hydrideHCID 86646134HCID 86646134、化合物

生成物 1

HCID 86646135HCID 86646135、化合物

試薬・触媒・溶媒 3

HCID 962Water溶媒HCID 8028Tetrahydrofuran溶媒3 回
HCID 8857
Ethyl Acetate
溶媒

反応条件

温度
0 °C

実験手順

A tetrahydrofuran (50 mL) solution of ethyl 2-sec-butylpent-4-enoate was added dropwise over 30 minutes to a tetrahydrofuran (120 mL) solution of lithium aluminum hydride (4.79 g, 126.3 mmol) cooled to 0° C., and the mixture was then stirred at 0° C. for 1 hour and then stirred at room temperature for 2 hours. The mixture was cooled again to 0° C. Ethyl acetate (55.4 mL), water (44.7 mL), tetrahydrofuran (83.1 mL), and sodium fluoride (53.0 g) were added thereto, and the mixture was stirred for 1.5 hours. The mixture was filtered through Celite to remove insoluble matter. Then, the solution was concentrated, and the residue was purified by silica gel column chromatography to obtain the compound of interest as a colorless oil substance (12.20 g, 69%).

後処理

  1. stirringstirred at room temperature for 2 hours
  2. temperatureThe mixture was cooled again to 0° C
  3. stirringthe mixture was stirred for 1.5 hours
  4. filtrationThe mixture was filtered through Celite
  5. customto remove insoluble matter
  6. concentrationThen, the solution was concentrated
  7. customthe residue was purified by silica gel column chromatography
  8. customto obtain the compound of interest as a colorless oil substance (12.20 g, 69%)

出典と根拠

ORDレコード
ord-766bc34c8f804b49ab278c55265f5925
出典データセット
uspto-grants-2011_05
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US07947738B2

反応ノート

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