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

HRID 1389178
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HRID 1389178 반응식
[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
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

5

반응물 4

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

생성물 1

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

실험 절차

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 ].

후처리

  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

출처 및 근거

ORD 기록
ord-6aaab0cd6b5845118555448361df9825
출처 데이터셋
uspto-grants-1981_01
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US04243683

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