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Chloroacetone → 2-Propanone, 1-((1-methyl-1H-tetrazol-5-yl)thio)-

HRID 728031
ノート
印刷プレビュー

反応式

HRID 728031 の反応式
O.[Na].[SH:3][C:4]1[N:8]([CH3:9])[N:7]=[N:6][N:5]=1.Cl[CH2:11][C:12](=[O:14])[CH3:13]>C(O)C>[CH3:9][N:8]1[C:4]([S:3][CH2:11][C:12]([CH3:13])=[O:14])=[N:5][N:6]=[N:7]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 6571ChloroacetoneHCID 178482031HCID 178482031、化合物

生成物 1

HCID 30619772-Propanone, 1-((1-methyl-1H-tetrazol-5-yl)thio)-

試薬・触媒・溶媒 1

HCID 702Ethanol溶媒

実験手順

To a solution of 3.12 g (0.02 mol) of 5-mercapto-1-methyltetrazole sodium salt hydrate in 60 ml of absolute ethanol was added dropwise, 2.06 g (0.2 mol) of chloroacetone. After stirring for 20 hours at room temperature, the ethanol was evaporated in vacuo. The residue was dissolved in methylene chloride and was washed with water and then brine prior to drying over Na2SO4. Evaporation of the methylene chloride solution gave 1-methyl-5-acetonylthiotetrazole that was purified by flash chromatography on silica gel to yield 0.94 g of the 5-acetonylthio-1-methyltetrazole product.

後処理

  1. customthe ethanol was evaporated in vacuo
  2. dissolutionThe residue was dissolved in methylene chloride
  3. washwas washed with water
  4. dry with materialbrine prior to drying over Na2SO4
  5. customEvaporation of the methylene chloride solution

出典と根拠

ORDレコード
ord-69deeb1296234ed9a1deaa3df3afcd02
出典データセット
uspto-grants-1991_09
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US05047416

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