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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 178454905、化合物

HRID 488074
ノート
印刷プレビュー

反応式

HRID 488074 の反応式
[CH2:1]([P:5]([CH2:21][CH2:22][CH2:23][CH3:24])[O:6]C1C=CC(C(C)(C)C)=CC=1C(C)(C)C)[CH2:2][CH2:3][CH3:4].O>C(#N)C>[CH2:1]([PH:5](=[O:6])[CH2:21][CH2:22][CH2:23][CH3:24])[CH2:2][CH2:3][CH3:4]
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

4

反応物 2

HCID 962WaterHCID 190917302.4-Di-tert.-butylphenyl dibutylphosphinite

生成物 1

HCID 178454905HCID 178454905、化合物収率 70%

試薬・触媒・溶媒 1

HCID 6342Acetonitrile溶媒

反応条件

温度
70 °C

実験手順

35 g (0.1 mol) of 2.4-di-tert.-butylphenyl dibutylphosphinite from Example 5 were reacted in 100 ml of acetonitrile with 2.0 g (0.11 mol) of water at 20° C., and the mixture was then stirred at 70° C. for 1 hour. The solvent was distilled off in vacuo, 50 ml of water and 100 ml of ethyl acetate were added, the phases were separated, and the organic phase was extracted two more times with 50 ml each of water. The combined aqueous phases were evaporated, and the residue distilled in vacuo, giving 10.2 g (70%) of a colorless liquid having a boiling point of 102° to 104° C./0.25 mbar.

後処理

  1. distillationThe solvent was distilled off in vacuo, 50 ml of water and 100 ml of ethyl acetate
  2. additionwere added
  3. customthe phases were separated
  4. extractionthe organic phase was extracted two more times with 50 ml each of water
  5. customThe combined aqueous phases were evaporated
  6. distillationthe residue distilled in vacuo

出典と根拠

ORDレコード
ord-de33f1bfd5ca4255822885dfb4d95eb7
出典データセット
uspto-grants-1994_03
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US05298644

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