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Diisopropylamine → 3-Ethoxy-4-ethoxycarbonylphenylacetic acid

HRID 2120002
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HRID 2120002 반응식
C([Li])CCC.C(NC(C)C)(C)C.CN(C)P(N(C)C)(N(C)C)=[O:16].[CH2:24]([O:26][C:27]1[CH:37]=[C:36]([CH3:38])[CH:35]=[CH:34][C:28]=1[C:29]([O:31][CH2:32][CH3:33])=[O:30])[CH3:25].[O:39]1[CH2:43]CCC1>CCOCC>[CH2:24]([O:26][C:27]1[CH:37]=[C:36]([CH2:38][C:43]([OH:39])=[O:16])[CH:35]=[CH:34][C:28]=1[C:29]([O:31][CH2:32][CH3:33])=[O:30])[CH3:25]
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참가 물질

7

반응물 5

HCID 7912DiisopropylamineHCID 8028Tetrahydrofuran2회HCID 12679HexamethylphosphoramideHCID 11816602Benzoic acid, 2-ethoxy-4-methyl-, ethyl esterHCID 178418339Butyllithium

생성물 1

HCID 101312123-Ethoxy-4-ethoxycarbonylphenylacetic acid수율 72.7%

시약·촉매·용매

1
HCID 3283Diethyl Ether용매

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온도
-30 °C

실험 절차

Under an atmosphere of nitrogen, n-butyllithium (25 ml, 15% w/w solution in hexane) was added to a solution of diisopropylamine (3.6 g) in tetrahydrofuran (30 ml) at −30° C. The mixture was stirred at −30° C. for 30 minutes, cooled to −75° C., and hexamethylphosphoramide (HMPA, 10 g) was added slowly. A solution of ethyl 2-ethoxy-4-methylbenzoate (5 g) in tetrahydrofuran (10 ml) was then added at −75° C. and the mixture was stirred for two hours. Carbon dioxide gas was then purged into the reaction mixture at −75° C. till complete decolorization. The reaction mixture was then stirred at −75 to −70° C. for 30 minutes and then brought to 10° C., diluted with water (50 ml), and extracted with ether. The aqueous layer was acidified with 10% aqueous sulphuric acid to pH ˜2 and extracted with dichloromethane. The combined dichloromethane layer was washed with water and concentrated in vacuo. The oily product so obtained was re-dissolved in ether (50 ml) and washed with water. The ethereal layer was then concentrated in vacuo to afford a thick oil which solidified on keeping at room temperature to afford 3-ethoxy-4-(ethoxycarbonyl)phenyl acetic acid 4.4 g (72.7%).

후처리

  1. temperaturecooled to −75° C.
  2. stirringthe mixture was stirred for two hours
  3. customCarbon dioxide gas was then purged into the reaction mixture at −75° C. till complete decolorization
  4. stirringThe reaction mixture was then stirred at −75 to −70° C. for 30 minutes
  5. custombrought to 10° C.
  6. additiondiluted with water (50 ml)
  7. extractionextracted with ether
  8. extractionextracted with dichloromethane
  9. washThe combined dichloromethane layer was washed with water
  10. concentrationconcentrated in vacuo
  11. customThe oily product so obtained
  12. washwashed with water
  13. concentrationThe ethereal layer was then concentrated in vacuo
  14. customto afford a thick oil which
  15. customon keeping at room temperature

출처 및 근거

ORD 기록
ord-bf07fa0f570b4aebb898b1dbecd1f3c6
출처 데이터셋
uspto-grants-2004_02
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US06686497B1

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