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Triethylamine → HCID 178476786、化合物

HRID 1654463
ノート
印刷プレビュー

反応式

HRID 1654463 の反応式
[CH2:1]([PH:8](=[O:10])[OH:9])[C:2]1[CH:7]=[CH:6][CH:5]=[CH:4][CH:3]=1.[CH2:11](N(CC)CC)[CH3:12].C(OC(Cl)=O)C>ClCCl>[CH2:11]([O:10][PH:8]([CH2:1][C:2]1[CH:7]=[CH:6][CH:5]=[CH:4][CH:3]=1)=[O:9])[CH3:12]
参加物実験手順後処理出典と根拠反応ノート

参加物

5

反応物 3

HCID 8471TriethylamineHCID 10928Ethyl chloroformateHCID 178527042HCID 178527042、化合物

生成物 1

HCID 178476786HCID 178476786、化合物

試薬・触媒・溶媒 1

HCID 6344Dichloromethane溶媒2 回

実験手順

13.34 g of benzylphosphinic acid are dissolved in 150 ml of dichloromethane, the solution is cooled to 5°, and 8.64 g of triethylamine are added dropwise. An exothermic reaction takes place. The mixture is cooled to 5° again, and 9.3 g of chloroformic acid ethyl ester are added dropwise within a period of 30 minutes. A precipitate forms in an exothermic reaction with the evolution of gas. The mixture is allowed to warm to room temperature and is then stirred at room temperature for 3 hours, taken up in dichloromethane and washed with water, and the organic solvent is removed. The crude product is distilled under a high vacuum, yielding benzylphosphinic acid ethyl ester having a boiling point of 96°-100 ° (5×10-6 bar).

後処理

  1. temperaturethe solution is cooled to 5°
  2. customAn exothermic reaction
  3. temperatureThe mixture is cooled to 5° again
  4. customA precipitate forms in an exothermic reaction with the evolution of gas
  5. washwashed with water
  6. customthe organic solvent is removed
  7. distillationThe crude product is distilled under a high vacuum

出典と根拠

ORDレコード
ord-dab986ddf5d84f188384442ce6aec55c
出典データセット
uspto-grants-1995_04
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US05407922

反応ノート

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