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Ammonium Hydroxide → HCID 66857363、化合物

HRID 252259
ノート
印刷プレビュー

反応式

HRID 252259 の反応式
[CH3:1][O:2][C:3]1[N:8]=[CH:7][C:6]([C:9]2[S:13][C:12]([S:14](Cl)(=[O:16])=[O:15])=[CH:11][C:10]=2[CH3:18])=[CH:5][CH:4]=1.[OH-].[NH4+:20]>CC(C)=O>[CH3:1][O:2][C:3]1[N:8]=[CH:7][C:6]([C:9]2[S:13][C:12]([S:14]([NH2:20])(=[O:16])=[O:15])=[CH:11][C:10]=2[CH3:18])=[CH:5][CH:4]=1
参加物実験手順後処理出典と根拠反応ノート

参加物

4

反応物 2

HCID 14923Ammonium HydroxideHCID 866167205-(6-Methoxy-pyridin-3-yl)-4-methyl-thiophene-2-sulfonyl chloride

生成物 1

HCID 66857363HCID 66857363、化合物

試薬・触媒・溶媒 1

HCID 180Acetone溶媒

実験手順

5-(6-Methoxy-pyridin-3-yl)-4-methyl-thiophene-2-sulfonyl chloride (0.19 g, 0.63 mmol) was dissolved in acetone (6 ml) and added dropwise to an aqueous ammonium hydroxide solution (25%, 1.2 ml). After 1 hour the solvent was removed under reduced pressure, the residue diluted with water and extracted with ethyl acetate (3×). The combined organic extracts were washed with water, brine, dried (MgSO4.2H2O), filtered and concentrated under reduced pressure to yield a crude that was purified over silica gel (n-heptane-ethyl acetate 1:2 to 2:1 v/v) to yield a beige solid: 0.12 g (62%), MS: m/e 283.0 (MH−).

後処理

  1. customAfter 1 hour the solvent was removed under reduced pressure
  2. additionthe residue diluted with water
  3. extractionextracted with ethyl acetate (3×)
  4. washThe combined organic extracts were washed with water, brine
  5. dry with materialdried (MgSO4.2H2O)
  6. filtrationfiltered
  7. concentrationconcentrated under reduced pressure
  8. customto yield a crude that
  9. customwas purified over silica gel (n-heptane-ethyl acetate 1:2 to 2:1 v/v)
  10. customto yield a beige solid

出典と根拠

ORDレコード
ord-649d919766c54de980b15d73a0e2ca24
出典データセット
uspto-grants-2011_01
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US07868030B2

反応ノート

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