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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
ノート
印刷プレビュー

反応式

HRID 1923607 の反応式
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]
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

5

反応物 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

生成物 1

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

試薬・触媒・溶媒 1

HCID 8857Ethyl Acetate
溶媒

反応条件

温度
90 °C

実験手順

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]+.

後処理

  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

出典と根拠

ORDレコード
ord-31d7e03547d943c7b4368c20fe4e0c57
出典データセット
uspto-grants-2012_05
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US08178522B2

反応ノート

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