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llms.txt · MCPガイドプライバシーポリシー · 利用規約 · サポートv1.8.0
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Water → 3-(2-Methyl-1,3-thiazol-5-yl)propan-1-ol

HRID 426936
ノート
印刷プレビュー

反応式

HRID 426936 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-].O>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

5

反応物 3

HCID 962WaterHCID 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

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

後処理

  1. filtrationwas then filtered
  2. washThe residue was washed with ethyl acetate
  3. dry with materialthe filtrate was dried over magnesium sulfate
  4. customevaporated to dryness
  5. customto obtain 8.4 g of raw product which

出典と根拠

ORDレコード
ord-b9c4a036ab144888a0bcdb8a71531fcb
出典データセット
uspto-grants-1979_10
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US04172137

反応ノート

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