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Sodium Hydroxide → alpha-Oxo-4-[4-(4-pyridinyl)butoxy]benzeneacetic acid

HRID 2225726
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HRID 2225726 반응식
C[O:2][C:3](=[O:23])[C:4](=[O:22])[C:5]1[CH:10]=[CH:9][C:8]([O:11][CH2:12][CH2:13][CH2:14][CH2:15][C:16]2[CH:21]=[CH:20][N:19]=[CH:18][CH:17]=2)=[CH:7][CH:6]=1.[OH-].[Na+]>CO.O>[O:22]=[C:4]([C:5]1[CH:6]=[CH:7][C:8]([O:11][CH2:12][CH2:13][CH2:14][CH2:15][C:16]2[CH:21]=[CH:20][N:19]=[CH:18][CH:17]=2)=[CH:9][CH:10]=1)[C:3]([OH:23])=[O:2]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

5

반응물 2

HCID 14798Sodium HydroxideHCID 54486867alpha-Oxo-4-[4-(4-pyridinyl)butoxy]benzeneacetic acid methyl ester

생성물 1

HCID 19004403alpha-Oxo-4-[4-(4-pyridinyl)butoxy]benzeneacetic acid수율 99.3%

시약·촉매·용매 2

HCID 887Methanol용매HCID 962Water용매

실험 절차

A mixture of alpha-oxo-4-[4-(4-pyridinyl)butoxy]benzeneacetic acid methyl ester (0.58 g) in hot methanol (10 mL) was treated with 1N sodium hydroxide (3.0 mL) and diluted with water. The organic solvent was removed under vacuum and the residue in water was washed with diethyl ether. The aqueous layer was concentrated to about 25 mL and chilled in ice. Cold 2N hydrochloric acid (1.5 mL) was added dropwise and the product was allowed to crystallize and was filtered and air dried. Recrystallization from water provided 0.55 g of alpha-oxo-4-[4-(4-pyridinyl)butoxy]benzeneacetic acid as a colorless solid, mp 198°-199° C.

후처리

  1. customThe organic solvent was removed under vacuum
  2. washthe residue in water was washed with diethyl ether
  3. concentrationThe aqueous layer was concentrated to about 25 mL
  4. temperaturechilled in ice
  5. additionCold 2N hydrochloric acid (1.5 mL) was added dropwise
  6. customto crystallize
  7. filtrationwas filtered
  8. customair dried
  9. customRecrystallization from water

출처 및 근거

ORD 기록
ord-51b1c0b45d4a43d1a354e4da7ef85d8b
출처 데이터셋
uspto-grants-1994_09
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US05344843

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