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2-Amino-5-methylpyridine → 2-aMino-5-Methylpyridine-3-sulfonyl chloride

HRID 1768554
ノート
印刷プレビュー

反応式

HRID 1768554 の反応式
[NH2:1][C:2]1[CH:7]=[CH:6][C:5]([CH3:8])=[CH:4][N:3]=1.[Cl:9][S:10](O)(=[O:12])=[O:11].C(=O)(O)[O-].[Na+]>>[NH2:1][C:2]1[C:7]([S:10]([Cl:9])(=[O:12])=[O:11])=[CH:6][C:5]([CH3:8])=[CH:4][N:3]=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

4

反応物 3

HCID 153482-Amino-5-methylpyridineHCID 24638Chlorosulfonic acidHCID 516892Sodium Bicarbonate

生成物 1

HCID 189487872-aMino-5-Methylpyridine-3-sulfonyl chloride収率 70%

反応条件

温度
140 °C

実験手順

Solid 2-amino-5-picoline (10.8 g, 0.10 mol) was added portionwise to chlorosulfonic acid (66 mL, 1.0 mol) at ambient temperature over 5 minutes. When the addition was complete, the mixture was warmed to 140° C. and stirred at that temperature for 2 hours. During the heating period gas evolution was initially rapid and ceased completely after 2 hours. The mixture was then cooled to room temperature and poured onto 2 liters of ice. Solid sodium bicarbonate was added to the resulting solution to adjust the pH to about 7.0. The solid product that precipitated was collected and rinsed with a small amount of cold ethanol. The solid was then dissolved in one liter of hot chloroform, the resulting solution was dried (magnesium sulfate), and the solution was concentrated to a volume of about 100 mL. The solid product that formed was collected, the mother liquor was concentrated to 20 mL and a second crop was collected. The solid products were combined to give the title compound (14.4 g, 70 %); m.p. 16°-166° C.

後処理

  1. additionWhen the addition
  2. waitceased completely after 2 hours
  3. temperatureThe mixture was then cooled to room temperature
  4. customThe solid product that precipitated
  5. customwas collected
  6. washrinsed with a small amount of cold ethanol
  7. dissolutionThe solid was then dissolved in one liter of hot chloroform
  8. dry with materialthe resulting solution was dried (magnesium sulfate)
  9. concentrationthe solution was concentrated to a volume of about 100 mL
  10. customThe solid product that formed
  11. customwas collected
  12. concentrationthe mother liquor was concentrated to 20 mL
  13. customa second crop was collected

出典と根拠

ORDレコード
ord-5eeb73fc862140c9846a967262927b7c
出典データセット
uspto-grants-1995_01
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US05378704

反応ノート

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