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Acetic Acid → 4-Methyl-2-(pyridin-3-yl)-1,3-thiazole-5-carboxylic acid

HRID 443556
ノート
印刷プレビュー

反応式

HRID 443556 の反応式
[OH-].[Na+].[CH3:3][C:4]1[N:5]=[C:6]([C:14]2[CH:15]=[N:16][CH:17]=[CH:18][CH:19]=2)[S:7][C:8]=1[C:9]([O:11]CC)=[O:10].Cl.C(O)(=O)C>O.C(O)C>[CH3:3][C:4]1[N:5]=[C:6]([C:14]2[CH:15]=[N:16][CH:17]=[CH:18][CH:19]=2)[S:7][C:8]=1[C:9]([OH:11])=[O:10]
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 176Acetic AcidHCID 313Hydrochloric AcidHCID 14798Sodium HydroxideHCID 619088Ethyl 4-methyl-2-(pyridin-3-yl)-1,3-thiazole-5-carboxylate

生成物 1

HCID 27634894-Methyl-2-(pyridin-3-yl)-1,3-thiazole-5-carboxylic acid収率 96%

試薬・触媒・溶媒 2

HCID 702Ethanol
溶媒
HCID 962Water溶媒

実験手順

A solution of sodium hydroxide (22 g. 0.55 mole) in water (300 ml.) was mixed with a solution of ethyl 4-methyl-2-(3-pyridyl)-5-thiazolecarboxylate (124 g., 0.50 mole) in 95% ethanol (150 ml.). The mixture was heated and stirred for about ten minutes on a steam bath, and then allowed to stand for one hour without further heating. When the ice-cooled reaction mixture was neutralized with dilute hydrochloric acid and acidified with acetic acid, a thick precipitate of finely divided white solid was obtained. The solid was collected by filtration, washed thoroughly with water, and dried in an oven at 110° C. The product (106 g., 96% yield) melted with decomposition at 249°-250° C.

後処理

  1. temperatureThe mixture was heated
  2. customreaction mixture
  3. customa thick precipitate of finely divided white solid was obtained
  4. filtrationThe solid was collected by filtration
  5. washwashed thoroughly with water
  6. customdried in an oven at 110° C
  7. custommelted with decomposition at 249°-250° C.

出典と根拠

ORDレコード
ord-95388d44cd2845409a19afc34b601efa
出典データセット
uspto-grants-1981_04
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US04260765

反応ノート

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