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Hydrochloric Acid → 6-Methylpyridine-3-sulfonyl chloride

HRID 1012517
ノート
印刷プレビュー

反応式

HRID 1012517 の反応式
[CH3:1][C:2]1[N:7]=[CH:6][C:5](N)=[CH:4][CH:3]=1.[ClH:9].N([O-])=O.[Na+].[S:14]([O-:17])(O)=[O:15].[Na+]>O.S([O-])([O-])(=O)=O.[Cu+2]>[CH3:1][C:2]1[N:7]=[CH:6][C:5]([S:14]([Cl:9])(=[O:17])=[O:15])=[CH:4][CH:3]=1
参加物実験手順後処理出典と根拠反応ノート

参加物

7

反応物 4

HCID 313Hydrochloric Acid2 回HCID 2433135-Amino-2-methylpyridineHCID 23665763Sodium BisulfiteHCID 23668193Sodium Nitrite

生成物 1

HCID 223987146-Methylpyridine-3-sulfonyl chloride収率 15%

試薬・触媒・溶媒 2

HCID 24462Copper Sulfate
触媒
HCID 962Water溶媒2 回

実験手順

To a mixture of 6-methylpyridine-3-amine (449 mg) and concentrated hydrochloric acid (5 mL) was added a solution of sodium nitrite (857 mg) in water (2 mL) at 0° C., and the mixture was stirred at the same temperature for 10 min. To the mixture was added a solution of concentrated hydrochloric acid (2.5 mL), copper sulfate (69 mg) and sodium hydrogen sulfite (5.08 g) in water (8 mL) at 0° C., and the mixture was stirred at room temperature for 30 min. The reaction mixture was extracted with ethyl acetate. The extract was washed with saturated brine, dried over anhydrous magnesium sulfate, and concentrated under reduced pressure. The residue was purified by silica gel column chromatography (eluent:hexane-ethyl acetate=10:1) to give the title compound as a pale-yellow solid (yield 0.12 g, 15%).

後処理

  1. stirringthe mixture was stirred at room temperature for 30 min
  2. extractionThe reaction mixture was extracted with ethyl acetate
  3. washThe extract was washed with saturated brine
  4. dry with materialdried over anhydrous magnesium sulfate
  5. concentrationconcentrated under reduced pressure
  6. customThe residue was purified by silica gel column chromatography (eluent:hexane-ethyl acetate=10:1)

出典と根拠

ORDレコード
ord-f0b66a6e841c4bbea4494f66ff0b766e
出典データセット
uspto-grants-2011_07
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US07977488B2

反応ノート

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