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Potassium Carbonate → N-[4-(Hydroxymethyl)-1,3-thiazol-2-YL]acetamide

HRID 1246420
ノート
印刷プレビュー

反応式

HRID 1246420 の反応式
C([O:4][CH2:5][C:6]1[N:7]=[C:8]([NH:11][C:12](=[O:14])[CH3:13])[S:9][CH:10]=1)(=O)C.C(=O)([O-])[O-].[K+].[K+]>CO>[OH:4][CH2:5][C:6]1[N:7]=[C:8]([NH:11][C:12](=[O:14])[CH3:13])[S:9][CH:10]=1
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 11430Potassium CarbonateHCID 14931747(2-Acetamido-1,3-thiazol-4-yl)methyl acetate

生成物 1

HCID 14931748N-[4-(Hydroxymethyl)-1,3-thiazol-2-YL]acetamide収率 94.7%

試薬・触媒・溶媒 1

HCID 887Methanol溶媒

実験手順

A mixture of (2-(acetylamino)-1,3-thiazol-4-yl)methyl acetate (46 g) and potassium carbonate (30 g) in methanol (640 ml) was stirred for 3 hours at ambient temperature. The reaction mixture was concentrated in vacuo. The residue was diluted with chloroform, and the insoluble material was filtered off. The resulting solution was purified by flash column chromatography on silica-gel with methanol/chloroform (1/99). The resulted solid was collected by filtration with isopropyl ether to give N-(4-(hydroxymethyl)-1,3-thiazol-2-yl)acetamide (35 g) as white crystals.

後処理

  1. concentrationThe reaction mixture was concentrated in vacuo
  2. additionThe residue was diluted with chloroform
  3. filtrationthe insoluble material was filtered off
  4. customThe resulting solution was purified by flash column chromatography on silica-gel with methanol/chloroform (1/99)
  5. filtrationThe resulted solid was collected by filtration with isopropyl ether

出典と根拠

ORDレコード
ord-e25449450da046fc98a4239639a3803e
出典データセット
uspto-grants-2006_10
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US07125901B2

反応ノート

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