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

HRID 443556
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HRID 443556 반응식
[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]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

7

반응물 4

HCID 176Acetic AcidHCID 313Hydrochloric AcidHCID 14798Sodium HydroxideHCID 619088Ethyl 4-methyl-2-(pyridin-3-yl)-1,3-thiazole-5-carboxylate

생성물 1

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

시약·촉매·용매 2

HCID 702
Ethanol
용매
HCID 962Water용매

실험 절차

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.

후처리

  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.

출처 및 근거

ORD 기록
ord-95388d44cd2845409a19afc34b601efa
출처 데이터셋
uspto-grants-1981_04
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US04260765

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