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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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Imidazole → HCID 12786212、化合物

HRID 126730
ノート
印刷プレビュー

反応式

HRID 126730 の反応式
[OH:1][CH2:2][C:3](=[O:8])[CH2:4][CH2:5][CH2:6][CH3:7].CN(C)C=O.N1C=CN=C1.Cl[Si:20]([CH2:25][CH3:26])([CH2:23][CH3:24])[CH2:21][CH3:22]>O>[CH2:21]([Si:20]([CH2:25][CH3:26])([CH2:23][CH3:24])[O:1][CH2:2][C:3](=[O:8])[CH2:4][CH2:5][CH2:6][CH3:7])[CH3:22]
参加物実験手順後処理出典と根拠反応ノート

参加物

6

反応物 4

HCID 795ImidazoleHCID 6228DimethylformamideHCID 13819ChlorotriethylsilaneHCID 1255690473397-68-9

生成物 1

HCID 12786212HCID 12786212、化合物

試薬・触媒・溶媒 1

HCID 962Water溶媒

実験手順

To a solution of the crude 1-hydroxy-hexan-2-one (prepared in Example 1) in 80 ml. of dimethylformamide at 0° C. is added with stirring, 40.8 g. of imidazole and 45.21 g. of chlorotriethylsilane. The mixture is stirred at 0° C. for 5 minutes and then at room temperature overnight, then poured into cold water and extracted with petroleum ether. The petroleum ether solution is washed with water, then saturated sodium bicarbonate solution and then dried over magnesium sulfate. The solvent is removed and the residue is distilled. The fraction boiling at 95°-103° C. (0.7 mm.) is collected giving the desired product as a cloudy colorless liquid.

後処理

  1. stirringThe mixture is stirred at 0° C. for 5 minutes
  2. extractionextracted with petroleum ether
  3. washThe petroleum ether solution is washed with water
  4. dry with materialsaturated sodium bicarbonate solution and then dried over magnesium sulfate
  5. customThe solvent is removed
  6. distillationthe residue is distilled
  7. customThe fraction boiling at 95°-103° C. (0.7 mm.) is collected

出典と根拠

ORDレコード
ord-cd9d328cb59b4ef2ab489306b8bde561
出典データセット
uspto-grants-1981_03
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US04254036

反応ノート

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