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Ethanol → Ethyl 3-(3-(trifluoromethyl)phenyl)propanoate

HRID 1389178
ノート
印刷プレビュー

反応式

HRID 1389178 の反応式
[F:1][C:2]([F:15])([F:14])[C:3]1[CH:4]=[C:5]([CH2:9][CH2:10][C:11]([OH:13])=[O:12])[CH:6]=[CH:7][CH:8]=1.S(=O)(=O)(O)O.O.[CH2:22](O)[CH3:23]>>[F:1][C:2]([F:14])([F:15])[C:3]1[CH:4]=[C:5]([CH2:9][CH2:10][C:11]([O:13][CH2:22][CH3:23])=[O:12])[CH:6]=[CH:7][CH:8]=1
参加物実験手順後処理出典と根拠反応ノート

参加物

5

反応物 4

HCID 702EthanolHCID 962WaterHCID 1118Sulfuric AcidHCID 27776833-(3-Trifluoromethylphenyl)propanoic acid

生成物 1

HCID 11849913Ethyl 3-(3-(trifluoromethyl)phenyl)propanoate

実験手順

A solution of 3-(3-trifluoromethylphenyl)propionic acid (13.6 g) in anhydrous ethanol (25 ml) containing concentrated sulphuric acid (1.5 ml) was heated at reflux for 24 hours and was then poured into water (100 ml). The mixture was extracted with diethyl ether and the ethereal extract was washed with water, with aqueous sodium carbonate solution (2 N), and with water, then dried over magnesium sulphate and evaporated. The resulting residue was distilled, to give ethyl 3-(3-trifluoromethylphenyl)propionate (11.5 g) in the form of a colourless oil, b.p. 133°-135° C./17 mm Hg. [elemental analysis: C, 58.6; H, 5.2%. C12H13F3O2 requires C, 58.5; H, 5.3%. νmax 1125, 1170, 1330 and 1740 cm-1 ].

後処理

  1. temperaturewas heated
  2. temperatureat reflux for 24 hours
  3. extractionThe mixture was extracted with diethyl ether
  4. extractionthe ethereal extract
  5. washwas washed with water, with aqueous sodium carbonate solution (2 N)
  6. dry with materialwith water, then dried over magnesium sulphate
  7. customevaporated
  8. distillationThe resulting residue was distilled

出典と根拠

ORDレコード
ord-6aaab0cd6b5845118555448361df9825
出典データセット
uspto-grants-1981_01
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US04243683

反応ノート

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