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Tetraethyl (phenoxymethylene)-bisphosphonate → (Phenoxymethylene)-bisphosphonic acid

HRID 569606
ノート
印刷プレビュー

反応式

HRID 569606 の反応式
[O:1]([CH:8]([P:17](=[O:24])([O:21]CC)[O:18]CC)[P:9](=[O:16])([O:13]CC)[O:10]CC)[C:2]1[CH:7]=[CH:6][CH:5]=[CH:4][CH:3]=1>Cl>[O:1]([CH:8]([P:17](=[O:18])([OH:21])[OH:24])[P:9](=[O:10])([OH:13])[OH:16])[C:2]1[CH:3]=[CH:4][CH:5]=[CH:6][CH:7]=1
参加物実験手順後処理出典と根拠反応ノート

参加物

3

反応物 1

HCID 54483224Tetraethyl (phenoxymethylene)-bisphosphonate

生成物 1

HCID 9816823(Phenoxymethylene)-bisphosphonic acid

試薬・触媒・溶媒 1

HCID 313Hydrochloric Acid溶媒

実験手順

A mixture of tetraethyl (phenoxymethylene)-bisphosphonate (20 g) and 6N hydrochloric acid (150 ml) was refluxed overnight and the resulting solution was evaporated to dryness in vacuo. Residual hydrochloric acid was removed by repeated evaporation with absolute ethanol. The residue was taken up in acetone (7 ml) and ether (200 ml) was added. The crystalline product was filtered, washed with ether and dried in vacuo.

後処理

  1. temperaturewas refluxed overnight
  2. customthe resulting solution was evaporated to dryness in vacuo
  3. customResidual hydrochloric acid was removed
  4. customevaporation with absolute ethanol
  5. additionether (200 ml) was added
  6. filtrationThe crystalline product was filtered
  7. washwashed with ether
  8. customdried in vacuo

出典と根拠

ORDレコード
ord-fed28e7d18344f6e97ba7c2d9727c9ab
出典データセット
uspto-grants-1988_03
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US04732998

反応ノート

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