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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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Methyl chloroacetate → HCID 20475380、化合物

HRID 223415
ノート
印刷プレビュー

反応式

HRID 223415 の反応式
Cl[CH2:2][C:3]([O:5][CH3:6])=[O:4].[CH2:7]([NH:11][C:12](=S)[NH:13][NH2:14])[CH:8]([CH3:10])[CH3:9].O1CC[CH2:18][CH2:17]1>>[CH2:7]([NH:11][C:12]1[C:2]([C:3]([O:5][CH3:6])=[O:4])=[C:17]([CH3:18])[NH:14][N:13]=1)[CH:8]([CH3:10])[CH3:9]
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 3

HCID 7295Methyl chloroacetateHCID 8028TetrahydrofuranHCID 12367441HCID 12367441、化合物

生成物 1

HCID 20475380HCID 20475380、化合物

実験手順

15.1 g of methyl 2-chloroacetate is added to a suspension of 14.7 g of 4-isobutylthiosemicarbazide in 150 ml of tetrahydrofuran. The mixture is stirred for 30 minutes and then boiled. After stirring for a further hour at 65° C., the mixture is cooled, the precipitated solid is isolated and washed with acetone. The residue is dissolved hot in water, filtered off from the precipitated sulfur and, after cooling, aqueous ammonia solution is added. After suction filtering and drying the product, 3-isobutylamino-4-methoxycarbonyl-5-methylpyrazole is isolated; m.p. 100°-103° C.

後処理

  1. stirringAfter stirring for a further hour at 65° C.
  2. temperature
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
the mixture is cooled
  • customthe precipitated solid is isolated
  • washwashed with acetone
  • dissolutionThe residue is dissolved hot in water
  • filtrationfiltered off from the precipitated sulfur
  • temperatureafter cooling
  • additionaqueous ammonia solution is added
  • filtrationAfter suction filtering
  • customdrying the product
  • 出典と根拠

    ORDレコード
    ord-05592d293d8943b9b185209c69665f72
    出典データセット
    uspto-grants-1982_10
    DOI
    10.6084/m9.figshare.5104873.v1
    特許番号
    US04354031

    反応ノート

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