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HCID 20388954、化合物 → 3-(2-Methyl-1,3-thiazol-5-yl)propan-1-ol

HRID 616379
ノート
印刷プレビュー

反応式

HRID 616379 の反応式
[CH3:1][C:2]1[S:3][C:4]([CH2:7][CH2:8][C:9](OC)=[O:10])=[CH:5][N:6]=1.[H-].[Al+3].[Li+].[H-].[H-].[H-]>O1CCCC1>[CH3:1][C:2]1[S:3][C:4]([CH2:7][CH2:8][CH2:9][OH:10])=[CH:5][N:6]=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 20388954HCID 20388954、化合物HCID 21226445Aluminium lithium hydride

生成物 1

HCID 203889553-(2-Methyl-1,3-thiazol-5-yl)propan-1-ol収率 69.2%

試薬・触媒・溶媒 1

HCID 8028Tetrahydrofuran溶媒3 回

実験手順

10.9 g of methyl 2-methyl-5-thiazole-propanoate in 70 ml of tetrahydrofuran was slowly added with stirring at 10°-15° C to a mixture of 125 ml of tetrahydrofuran and 3.42 g of lithium aluminum hydride at 10° C and the mixture was stirred for about 30 minutes. Then, tetrahydrofuran containing 20% water was slowly added and the mixture was filtered. The filter was washed with ethyl acetate and the filtrate was dried over magnesium sulfate and concentrated under reduced pressure to obtain 8.4 g of raw product which was rectified under reduced pressure to obtain 6.4g of 2-methyl-5-thiazole propanol with a boiling point of 106° C under 0.05 mm Hg.

後処理

  1. filtrationthe mixture was filtered
  2. washThe filter was washed with ethyl acetate
  3. dry with materialthe filtrate was dried over magnesium sulfate
  4. concentrationconcentrated under reduced pressure
  5. customto obtain 8.4 g of raw product which

出典と根拠

ORDレコード
ord-f329d76be58645709fdad2cefed6c71b
出典データセット
uspto-grants-1978_02
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US04073919

反応ノート

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このページの内容参加物実験手順後処理出典と根拠反応ノート