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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 → HCID 21470408、化合物

HRID 2294750
ノート
印刷プレビュー

反応式

HRID 2294750 の反応式
C1(C)C=CC(S(O[CH2:11][CH2:12][CH2:13][CH2:14][CH2:15][CH2:16][CH2:17][CH2:18][CH2:19][CH:20]=[CH2:21])(=O)=O)=CC=1.O[C:24]1[CH:29]=[CH:28][C:27]([C:30]2[CH:35]=[CH:34][C:33]([OH:36])=[CH:32][CH:31]=2)=[CH:26][CH:25]=1.[H-].[Na+].[OH2:39]>C(O)CCC>[CH2:21]([O:36][C:33]1[CH:34]=[CH:35][C:30]([C:27]2[CH:28]=[CH:29][CH:24]=[CH:25][CH:26]=2)=[C:31]([OH:39])[CH:32]=1)[CH2:20][CH2:19][CH2:18][CH2:17][CH2:16][CH2:15][CH2:14][CH2:13][CH:12]=[CH2:11]
参加物反応条件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 962WaterHCID 71124,4'-DihydroxybiphenylHCID 24758Sodium hydrideHCID 11141895HCID 11141895、化合物

生成物 1

HCID 21470408HCID 21470408、化合物収率 47.6%

試薬・触媒・溶媒 1

HCID 2631-Butanol溶媒3 回

反応条件

温度
110 °C

実験手順

The above-prepared 2.60 g (8.02 mM) of 10-undecenyl p-toluenesulfonate, 3.0 g (16.0 mM) of dihydroxybiphenyl and 3 ml of butanol were mixed and sufficiently stirred. To the mixture, a solution of 0.41 g (9.74 mM) of sodium hydride in 6 ml of butanol was added, followed by heat-refluxing for 7 hours at 110° C. After the reaction, the reaction mixture was subjected to distilling-off of butanol and addition of water, followed by extraction with ether to obtain an extract. The extract was dried with anhydrous sodium sulfate, followed by distilling-off of ether and purification by column chromatography (eluent: methylene chloride) to obtain 1.55 g (3.82 mM) of p-(10-undecenyl)oxyhydroxybiphenyl (Yield: 47.6%).

後処理

  1. customAfter the reaction
  2. extractionfollowed by extraction with ether
  3. customto obtain an extract
  4. dry with materialThe extract was dried with anhydrous sodium sulfate
  5. distillationfollowed by distilling-off of ether and purification by column chromatography (eluent: methylene chloride)

出典と根拠

ORDレコード
ord-7427014f914c414fb694d6456fac1cd8
出典データセット
uspto-grants-1997_11
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US05690858

反応ノート

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このページの内容参加物反応条件実験手順後処理出典と根拠反応ノート