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Ethanol → Ethyl 3-(3-hydroxyphenyl)propanoate

HRID 1925234
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HRID 1925234 반응식
[OH:1][C:2]1[CH:3]=[C:4]([CH:8]([CH3:12])C(O)=O)[CH:5]=[CH:6][CH:7]=1.[OH2:13].[C:14]1([CH3:24])C=CC(S(O)(=O)=O)=CC=1.[CH2:25]([OH:27])C>>[OH:1][C:2]1[CH:3]=[C:4]([CH2:8][CH2:12][C:25]([O:27][CH2:14][CH3:24])=[O:13])[CH:5]=[CH:6][CH:7]=1
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참가 물질

4

반응물 3

HCID 702EthanolHCID 521998p-Toluenesulfonic acid monohydrateHCID 124468532-(3-Hydroxyphenyl)propionic acid, (+-)-

생성물 1

HCID 15197885Ethyl 3-(3-hydroxyphenyl)propanoate

실험 절차

A solution of 3-Hydroxyphenylpropanoic acid (25 g, 150.60 mmol) and p-Toluenesulfonic acid monohydrate (3.80 g, 20 mmol) in abs ethanol (250 ml) was refluxed for 4 hours or until all the starting material is consumed. The reaction mixture was concentrated, diluted with ethyl acetate and washed with water. The organic layer was dried over Na2SO4, filtered, concentrated, and purified by flash chromatography on a silica gel column (hex:ethyl acetate 2:1) to give the title compound.

후처리

  1. customis consumed
  2. concentrationThe reaction mixture was concentrated
  3. additiondiluted with ethyl acetate
  4. washwashed with water
  5. dry with materialThe organic layer was dried over Na2SO4
  6. filtrationfiltered
  7. concentrationconcentrated
  8. custompurified by flash chromatography on a silica gel column (hex:ethyl acetate 2:1)

출처 및 근거

ORD 기록
ord-20b135e5414c4a0c9a10063968dc63f0
출처 데이터셋
uspto-grants-2012_05
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08178675B2

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