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Dimethyl Sulfone → HCID 67997695、化合物

HRID 1425969
ノート
印刷プレビュー

反応式

HRID 1425969 の反応式
[Br:1][C:2]1[CH:3]=[CH:4][C:5](F)=[N:6][CH:7]=1.C[Si](C)(C)[N-][Si](C)(C)C.[Na+].[CH3:19][S:20]([CH3:23])(=[O:22])=[O:21]>O1CCCC1>[Br:1][C:2]1[CH:3]=[CH:4][C:5]([CH2:19][S:20]([CH3:23])(=[O:22])=[O:21])=[N:6][CH:7]=1
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

5

反応物 3

HCID 6213Dimethyl SulfoneHCID 2724254Sodium bis(trimethylsilyl)amideHCID 27831685-Bromo-2-fluoropyridine

生成物 1

HCID 67997695HCID 67997695、化合物

試薬・触媒・溶媒 1

HCID 8028Tetrahydrofuran溶媒2 回

反応条件

温度
-17 °C

実験手順

5-Bromo-2-fluoro-pyridine (2.00 g) dissolved in tetrahydrofuran (20 mL) was added dropwise to a solution of sodium hexamethyldisilazide (2 mol/L in tetrahydrofuran, 28.5 mL) in tetrahydrofuran (20 mL) cooled to ca. −17° C. Dimethylsulfone (4.30 g) was added and stirring continued in the cooling bath for 1 h. The cooling bath was then removed and the solution was stirred at room temperature for one more h. Aqueous NH4Cl solution and brine were added and the resulting mixture was extracted with ethyl acetate. The combined extracts were dried (MgSO4) and the solvent was evaporated. The residue was treated with little ethyl acetate to precipitate the title compound. Yield: 1.73 g (63% of theory); LC (method 3): tR=2.01 min; Mass spectrum (ESI+): m/z=250/252 (Br) [M+H]+.

後処理

  1. customThe cooling bath was then removed
  2. stirringthe solution was stirred at room temperature for one more h
  3. additionAqueous NH4Cl solution and brine were added
  4. extractionthe resulting mixture was extracted with ethyl acetate
  5. dry with materialThe combined extracts were dried (MgSO4)
  6. customthe solvent was evaporated
  7. additionThe residue was treated with little ethyl acetate
  8. customto precipitate the title compound

出典と根拠

ORDレコード
ord-d9bb245521ed461dbdcfcf58d0b9f976
出典データセット
uspto-grants-2015_01
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US08933072B2

反応ノート

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