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Sulfuric Acid → 2-[(E)-2-(3-Butyl-5-methyl-isoxazol-4-yl)-vinyl]-4-methyl-thiazole-5-carboxylic acid methyl ester

HRID 1923607
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HRID 1923607 반응식
S(=O)(=O)(O)O.[CH3:6][O:7][C:8]([C:10]1[S:14][C:13]([CH2:15][CH:16]([C:18]2[C:19]([CH2:24][CH2:25][CH2:26][CH3:27])=[N:20][O:21][C:22]=2[CH3:23])O)=[N:12][C:11]=1[CH3:28])=[O:9].[OH-].[Na+]>C(OCC)(=O)C>[CH3:6][O:7][C:8]([C:10]1[S:14][C:13](/[CH:15]=[CH:16]/[C:18]2[C:19]([CH2:24][CH2:25][CH2:26][CH3:27])=[N:20][O:21][C:22]=2[CH3:23])=[N:12][C:11]=1[CH3:28])=[O:9]
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참가 물질

5

반응물 3

HCID 1118Sulfuric AcidHCID 14798Sodium HydroxideHCID 666436972-[2-(3-Butyl-5-methyl-isoxazol-4-yl)-2-hydroxy-ethyl]-4-methyl-thiazole-5-carboxylic acid methyl ester

생성물 1

HCID 666436512-[(E)-2-(3-Butyl-5-methyl-isoxazol-4-yl)-vinyl]-4-methyl-thiazole-5-carboxylic acid methyl ester수율 94.1%

시약·촉매·용매 1

HCID 8857Ethyl Acetate
용매

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온도
90 °C

실험 절차

Concentrated sulfuric acid (85 mL) was added to 2-[2-(3-butyl-5-methyl-isoxazol-4-yl)-2-hydroxy-ethyl]-4-methyl-thiazole-5-carboxylic acid methyl ester (9.0 g, 26.6 mmol) then the mixture was heated at 90° C. for 2 h. The solution was carefully dropped into 2N sodium hydroxide (1580 mL) and ethyl acetate (100 mL) saturated sodium bicarbonate was added until pH 10 was reached. The reaction mixture was extracted with ethyl acetate then the combined organic extracts were dried, filtered and concentrated, to give the title compound (8.02 g, 94%) as a yellow oil that was used directly without further purification. MS: m/e=321.2 [M+H]+.

후처리

  1. additionwas added until pH 10
  2. extractionThe reaction mixture was extracted with ethyl acetate
  3. customthe combined organic extracts were dried
  4. filtrationfiltered
  5. concentrationconcentrated

출처 및 근거

ORD 기록
ord-31d7e03547d943c7b4368c20fe4e0c57
출처 데이터셋
uspto-grants-2012_05
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08178522B2

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