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Lithium hydroxide, monohydrate → 2-(3-(Pyridin-2-yl)phenyl)acetic acid

HRID 1058573
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HRID 1058573 반응식
C[O:2][C:3](=[O:17])[CH2:4][C:5]1[CH:10]=[CH:9][CH:8]=[C:7]([C:11]2[CH:16]=[CH:15][CH:14]=[CH:13][N:12]=2)[CH:6]=1.O[Li].O>C1COCC1.O>[N:12]1[CH:13]=[CH:14][CH:15]=[CH:16][C:11]=1[C:7]1[CH:6]=[C:5]([CH2:4][C:3]([OH:17])=[O:2])[CH:10]=[CH:9][CH:8]=1
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참가 물질

5

반응물 2

HCID 168937Lithium hydroxide, monohydrateHCID 543647723-(2-Pyridyl)-phenyl acetic acid methyl ester

생성물 1

HCID 120760552-(3-(Pyridin-2-yl)phenyl)acetic acid수율 106.4%

시약·촉매·용매 2

HCID 962Water용매HCID 8028Tetrahydrofuran용매

실험 절차

To a solution of the compound of 3-(2-pyridyl)-phenyl acetic acid methyl ester (3.8 g, 16.7 mmol) in THF (50 mL) was added a solution of LiOH.H2O (780.2 mg, 18.6 mmol) in H2O (10 mL). The reaction was stirred at room temperature until TLC analysis indicated the complete consumption of starting material (2 h). The reaction mixture was concentrated to remove THF, then neutralized to pH=7 by the addition of IN HCl, diluted with brine (50 mL), and washed with CHCl3 (100 mL) The aqueous layer was readjusted back to pH=7 by the addition on IN NaOH and washed with fresh CHCl3 (100 mL). After repeating this procedure once more, the organic layers were combined, dried, filtered (MgSO4) and concentrated to give 3.79 g of the title compound: MS (ES+) 214.3 (MH+).

후처리

  1. customthe complete consumption of starting material (2 h)
  2. concentrationThe reaction mixture was concentrated
  3. customto remove THF
  4. additionneutralized to pH=7 by the addition of IN HCl
  5. additiondiluted with brine (50 mL)
  6. washwashed with CHCl3 (100 mL) The aqueous layer
  7. additionwas readjusted back to pH=7 by the addition on IN NaOH
  8. washwashed with fresh CHCl3 (100 mL)
  9. customdried
  10. filtrationfiltered (MgSO4)
  11. concentrationconcentrated

출처 및 근거

ORD 기록
ord-ecfd12dceb9446ba9a585d64b6072919
출처 데이터셋
uspto-grants-2003_02
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US06518267B1

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