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Sodium Bicarbonate → Ethyl (2-propyl-1,3-thiazol-5-yl)acetate

HRID 972835
ノート
印刷プレビュー

反応式

HRID 972835 の反応式
Br[CH:2]([CH2:8][CH:9]=O)[C:3]([O:5][CH2:6][CH3:7])=[O:4].[C:11]([NH2:16])(=[S:15])[CH2:12][CH2:13][CH3:14].C(=O)(O)[O-].[Na+]>ClC(Cl)C>[CH2:12]([C:11]1[S:15][C:8]([CH2:2][C:3]([O:5][CH2:6][CH3:7])=[O:4])=[CH:9][N:16]=1)[CH2:13][CH3:14]
参加物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 516892Sodium BicarbonateHCID 12454243ButanethioamideHCID 18668033Ethyl 2-bromo-4-oxo-butyrate

生成物 1

HCID 54320013Ethyl (2-propyl-1,3-thiazol-5-yl)acetate収率 73.3%

試薬・触媒・溶媒 1

HCID 63651,1-Dichloroethane溶媒

実験手順

A mixture of 20.6 g of ethyl 2-bromo-4-oxo-butyrate, 10.9 g of thiobutyramide and 400 ml of dichloroethane was refluxed under a nitrogen atmosphere which recycling the dehydrated condensate. The mixture was cooled and then mixed with 45 ml of a saturated sodium bicarbonate aqueous solution. The mixture was decanted and the organic phase was dried and evaporated to dryness. The liquid residue was chromatographed over silica gel and elution with a 8-2 cyclohexane-benzene mixture yielded 15.4 g of ethyl 2-propyl-5-thiazole-acetate. The IR spectrum in CHCl3 showed an ester carbonyl at 1737cm-1 and C=C at 1536cm-1

後処理

  1. temperaturewas refluxed under a nitrogen atmosphere which
  2. temperatureThe mixture was cooled
  3. customThe mixture was decanted
  4. customthe organic phase was dried
  5. customevaporated to dryness
  6. customThe liquid residue was chromatographed over silica gel and elution with a 8-2 cyclohexane-benzene mixture

出典と根拠

ORDレコード
ord-7972fdc278954c5f9728ea362ee147ab
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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