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Water → 2-Methoxymethyl-4-propyl-5-(4-aminobenzyl)thiazole

HRID 1613240
ノート
印刷プレビュー

反応式

HRID 1613240 の反応式
[CH3:1][O:2][CH2:3][C:4]1[S:5][C:6]([CH2:12][C:13]2[CH:18]=[CH:17][C:16]([N+:19]([O-])=O)=[CH:15][CH:14]=2)=[C:7]([CH2:9][CH2:10][CH3:11])[N:8]=1.O>CO.[Ni]>[CH3:1][O:2][CH2:3][C:4]1[S:5][C:6]([CH2:12][C:13]2[CH:14]=[CH:15][C:16]([NH2:19])=[CH:17][CH:18]=2)=[C:7]([CH2:9][CH2:10][CH3:11])[N:8]=1
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 2

HCID 962WaterHCID 19775540HCID 19775540、化合物

生成物 1

HCID 197755572-Methoxymethyl-4-propyl-5-(4-aminobenzyl)thiazole

試薬・触媒・溶媒 2

HCID 935Nickel触媒HCID 887Methanol溶媒

実験手順

0.9 of 2-methoxymethyl-4-propyl-5-(4-nitrobenzyl)thiazole in 50 ml of methanol is hydrogenated at normal pressure and room temperature in the presence of Raney nickel. After filtration of the catalyst and concentration of the filtrate, the brown oil obtained is taken up with acidified water. The aqueous phase is extracted with ether, rendered basic with dilute sodium hydroxide and extracted with ethyl acetate. The organic phase is dried and concentrated to give 0.5 g of 2-methoxymethyl-4-propyl-5-(4-aminobenzyl)thiazole in the form of an orange oil, which is used as such for the next step.

後処理

  1. filtrationAfter filtration of the catalyst and concentration of the filtrate
  2. customthe brown oil obtained
  3. extractionThe aqueous phase is extracted with ether
  4. extractionextracted with ethyl acetate
  5. customThe organic phase is dried
  6. concentrationconcentrated

出典と根拠

ORDレコード
ord-291153c75bb64ab7a281eea7dc8a7e34
出典データセット
uspto-grants-1993_03
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US05192781

反応ノート

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