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Water → 2-Propanone, 1-(1-oxopropoxy)-

HRID 1821141
ノート
印刷プレビュー

反応式

HRID 1821141 の反応式
[OH:1][CH2:2][C:3](=[O:5])[CH3:4].N1C=CC=CC=1.[C:12](Cl)(=[O:15])[CH2:13][CH3:14].O>C(OCC)(=O)C>[C:12]([O:1][CH2:2][C:3](=[O:5])[CH3:4])(=[O:15])[CH2:13][CH3:14]
参加物実験手順後処理出典と根拠反応ノート

参加物

6

反応物 4

HCID 962WaterHCID 1049PyridineHCID 8299HydroxyacetoneHCID 62324Propionyl chloride

生成物 1

HCID 30858602-Propanone, 1-(1-oxopropoxy)-収率 64.8%

試薬・触媒・溶媒 1

HCID 8857Ethyl Acetate溶媒

実験手順

To a solution of hydroxyacetone (190 g, 2.56 mol) and pyridine (210 ml, 2.6 mol) in ethyl acetate (1 L), propionyl chloride (197 g, 2.1 mol) was added dropwise at 5° C. The reaction liquid was stirred at room temperature for one hour, and then poured into water (700 ml). After phase separation, the organic layer was washed twice with a 1−N aqueous hydrochloric acid (700 ml), twice with water (700 ml), and once with saturated brine (500 ml), and dried over magnesium sulfate. After the magnesium sulfate was filtered out, the solvent was distilled off under reduced pressure, to obtain propionyloxyacetone (177 g, 1.36 mol). The thus-obtained propionyloxyacetone was used in the next process, without further purification.

このページの内容参加物実験手順後処理出典と根拠反応ノート

後処理

  1. customThe reaction liquid
  2. customAfter phase separation
  3. washthe organic layer was washed twice with a 1−N aqueous hydrochloric acid (700 ml), twice with water (700 ml)
  4. dry with materialonce with saturated brine (500 ml), and dried over magnesium sulfate
  5. filtrationAfter the magnesium sulfate was filtered out
  6. distillationthe solvent was distilled off under reduced pressure

出典と根拠

ORDレコード
ord-872fdbeccd164761bf96ebf45eab2455
出典データセット
uspto-grants-2009_10
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US07605276B2

反応ノート

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