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Potassium Hydroxide → 2-Propyl-5-thiazole-acetic acid

HRID 972836
ノート
印刷プレビュー

反応式

HRID 972836 の反応式
[CH2:1]([C:4]1[S:5][C:6]([CH2:9][C:10]([O:12]CC)=[O:11])=[CH:7][N:8]=1)[CH2:2][CH3:3].[OH-].[K+]>CO>[CH2:1]([C:4]1[S:5][C:6]([CH2:9][C:10]([OH:12])=[O:11])=[CH:7][N:8]=1)[CH2:2][CH3:3]
参加物実験手順後処理出典と根拠反応ノート

参加物

4

反応物 2

HCID 14797Potassium HydroxideHCID 54320013Ethyl (2-propyl-1,3-thiazol-5-yl)acetate

生成物 1

HCID 214055832-Propyl-5-thiazole-acetic acid収率 67%

試薬・触媒・溶媒 1

HCID 887Methanol溶媒

実験手順

A mixture of 2.13 g of ethyl 2-propyl-5-thiazole acetate, 11 ml of methanol and 1.1 ml of potassium hydroxide was stirred for 1 hour under a nitrogen atmosphere at room temperature and the methanol was distilled under reduced pressure. The residue was dissolved in 5 ml of water and 2 ml of concentrated hydrochloric acid and then 2.1 g of sodium acetate were added thereto. The mixture was extracted with methylene chloride and the organic extracts were dried and evaporated to dryness. The residue was crystallized from toluene to obtain 1.24g of 2-propyl-5-thiazole-acetic acid melting at 95° C.

後処理

  1. distillationthe methanol was distilled under reduced pressure
  2. dissolutionThe residue was dissolved in 5 ml of water
  3. addition2 ml of concentrated hydrochloric acid and then 2.1 g of sodium acetate were added
  4. extractionThe mixture was extracted with methylene chloride
  5. customthe organic extracts were dried
  6. customevaporated to dryness
  7. customThe residue was crystallized from toluene

出典と根拠

ORDレコード
ord-2648237ccd9e4539a84c3db7c59c2720
出典データセット
uspto-grants-1977_10
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US04053618

反応ノート

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