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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 689757、化合物

HRID 547242
ノート
印刷プレビュー

反応式

HRID 547242 の反応式
[NH2:1][C:2]1[CH:7]=[CH:6][CH:5]=[CH:4][C:3]=1[OH:8].[Cl-].[Li+].[C:11](Cl)(=[O:21])[C:12]1[CH:20]=[CH:19][CH:18]=[C:14]([C:15](Cl)=[O:16])[CH:13]=1.[OH2:23]>CN1C(=O)CCC1>[OH:8][C:3]1[CH:4]=[CH:5][CH:6]=[CH:7][C:2]=1[NH:1][C:11](=[O:21])[C:12]1[CH:20]=[CH:19][CH:18]=[C:14]([C:15]([NH:1][C:2]2[CH:7]=[CH:6][CH:5]=[CH:4][C:3]=2[OH:23])=[O:16])[CH:13]=1
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 962WaterHCID 58012-AminophenolHCID 7451Isophthaloyl chlorideHCID 433294Lithium Chloride

生成物 1

HCID 689757HCID 689757、化合物

試薬・触媒・溶媒 1

HCID 13387N-methyl-2-pyrrolidone溶媒

実験手順

In 260 mL of NMP were dissolved 27.548 g of o-aminophenol and 11.484 g of lithium chloride. To the solution was added 25 g of isophthaloyl chloride under ice-cooling, and the solution was further stirred at room temperature overnight. The reaction mixture was then poured into water, and the precipitation was filtered and washed with water. The obtained precipitation was dissolved in 500 mL of tetrahydrofuran again and dried over magnesium sulfate. The solvent was then evaporated off under a reduced pressure to obtain 40 g of N,N′-di(2-hydroxyphenyl)isophthalamide.

後処理

  1. temperaturecooling
  2. customthe precipitation
  3. filtrationwas filtered
  4. washwashed with water
  5. customThe obtained precipitation
  6. dissolutionwas dissolved in 500 mL of tetrahydrofuran again
  7. dry with materialdried over magnesium sulfate
  8. customThe solvent was then evaporated off under a reduced pressure

出典と根拠

ORDレコード
ord-c9c586e090e54369ac5af4d2b7fd9c24
出典データセット
uspto-grants-2011_05
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US07939241B2

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