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Water → 2-[(Methylsulfonyl)methyl]-5-[4-nitro-3-(tetrahydro-2H-pyran-4-yloxy)phenoxy]pyridine

HRID 1042116
ノート
印刷プレビュー

反応式

HRID 1042116 の反応式
F[C:2]1[CH:3]=[CH:4][C:5]([N+:15]([O-:17])=[O:16])=[C:6]([CH:14]=1)[O:7][CH:8]1[CH2:13][CH2:12][O:11][CH2:10][CH2:9]1.[CH3:18][S:19]([CH2:22][C:23]1[N:28]=[CH:27][C:26]([OH:29])=[CH:25][CH:24]=1)(=[O:21])=[O:20].C(=O)([O-])[O-].[K+].[K+].O>CN(C)C=O.CCCCCC.C(OCC)(=O)C>[CH3:18][S:19]([CH2:22][C:23]1[CH:24]=[CH:25][C:26]([O:29][C:2]2[CH:3]=[CH:4][C:5]([N+:15]([O-:17])=[O:16])=[C:6]([O:7][CH:8]3[CH2:13][CH2:12][O:11][CH2:10][CH2:9]3)[CH:14]=2)=[CH:27][N:28]=1)(=[O:21])=[O:20]
参加物反応条件実験手順後処理出典と根拠反応ノート

参加物

8

反応物 4

HCID 962WaterHCID 11430Potassium CarbonateHCID 533521804-(5-fluoro-2-nitrophenoxy)tetrahydro-2H-pyranHCID 667261886-[(Methylsulfonyl)methyl]pyridin-3-ol

生成物 1

HCID 667262242-[(Methylsulfonyl)methyl]-5-[4-nitro-3-(tetrahydro-2H-pyran-4-yloxy)phenoxy]pyridine収率 99.9%

試薬・触媒・溶媒 3

HCID 6228
Dimethylformamide
溶媒
HCID 8058Hexane溶媒
HCID 8857Ethyl Acetate溶媒

反応条件

温度
110 °C

実験手順

To a solution of 4-(5-fluoro-2-nitrophenoxy)tetrahydro-2H-pyran (13.6 g) and 6-[(methylsulfonyl)methyl]pyridin-3-ol (13.9 g) in N,N-dimethylformamide (300 mL) was added potassium carbonate (39 g), and the mixture was stirred at 110° C. for 2 hr. Water was added to the reaction solution, and the mixture was extracted with ethyl acetate. The organic layer was washed with saturated brine, dried over magnesium sulfate, filtered and concentrated under reduced pressure. The obtained crude product was subjected to silica gel column chromatography (ethyl acetate:hexane=0:100 to 50:50, volume ratio) to give the title compound (23 g, yield 95%) as a yellow solid.

後処理

  1. extractionthe mixture was extracted with ethyl acetate
  2. washThe organic layer was washed with saturated brine
  3. dry with materialdried over magnesium sulfate
  4. filtrationfiltered
  5. concentrationconcentrated under reduced pressure
  6. customThe obtained crude product

出典と根拠

ORDレコード
ord-e95e18d375c14e71b7b563f0cea6476c
出典データセット
uspto-grants-2013_10
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US08557805B2

反応ノート

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