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Boron trifluoride etherate → 1,1-Diethoxy-4,4-dimethoxypentan-3-one

HRID 2183868
ノート
印刷プレビュー

反応式

HRID 2183868 の反応式
B(F)(F)F.CCOCC.[CH:10]([O:17][CH2:18][CH3:19])([O:14][CH2:15][CH3:16])OCC.[CH3:20][O:21][C:22]([O:27][CH3:28])([CH3:26])[C:23](=[O:25])[CH3:24].C(N(CC)C(C)C)(C)C.C(=O)([O-])O.[Na+]>ClCCl>[CH2:18]([O:17][CH:10]([O:14][CH2:15][CH3:16])[CH2:24][C:23](=[O:25])[C:22]([O:27][CH3:28])([O:21][CH3:20])[CH3:26])[CH3:19]
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 5

HCID 8000Boron trifluoride etherateHCID 31214Ethyl orthoformateHCID 81531DiisopropylethylamineHCID 1408713,3-Dimethoxy-2-butanoneHCID 516892Sodium Bicarbonate

生成物 1

HCID 221807921,1-Diethoxy-4,4-dimethoxypentan-3-one収率 100%

試薬・触媒・溶媒 1

HCID 6344Dichloromethane溶媒2 回

反応条件

温度
-78 °C

実験手順

Boron trifluoride etherate (17.03 g, 120.0 mmol) was added drop-wise over 15 min to a cooled (−40° C.) solution of triethyl orthoformate (14.82 g, 100.0 mmol) in dichloromethane (50 ml). Stirring was continued for 10 min then the solution was transferred to an ice-water bath and stirred at 0° C. for 20 min. The mixture was cooled to −78° C., and 3,3-dimethoxy-2-butanone (6.61 g, 50.0 mmol) added followed by dropwise addition of N,N-diisopropylethylamine (19.39 g, 150.0 mmol) over 15 min. Stirring was continued for 1 h then the solution was poured onto a vigorously stirred mixture of saturated sodium hydrogencarbonate solution (500 ml) and dichloromethane (200 ml). The organic phase was separated, washed with ice-cold 1M sulfuric acid solution (2×500 ml) and ice-cold water (2×500 ml), dried over anhydrous sodium sulfate solution and evaporated to give 1,1-diethoxy-4,4-dimethoxypentan-3-one (11.72 g, 100%) as an orange oil.

後処理

  1. customthe solution was transferred to an ice-water bath
  2. stirringstirred at 0° C. for 20 min
  3. stirringStirring
  4. waitwas continued for 1 h
  5. customThe organic phase was separated
  6. washwashed with ice-cold 1M sulfuric acid solution (2×500 ml) and ice-cold water (2×500 ml)
  7. dry with materialdried over anhydrous sodium sulfate solution
  8. customevaporated

出典と根拠

ORDレコード
ord-6cad744632a24d94ab534eb6704fcd61
出典データセット
uspto-grants-2005_05
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US06900215B2

反応ノート

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