Water → Benzoylaminomethanephosphonic acid

HRID 466301

反応式

HRID 466301 の反応式
O[CH2:2][NH:3][C:4](=[O:11])[C:5]1[CH:10]=[CH:9][CH:8]=[CH:7][CH:6]=1.O=P[O:14][P:15]=[O:16].[OH2:17]>O1CCCC1>[C:4]([NH:3][CH2:2][P:15]([OH:16])(=[O:17])[OH:14])(=[O:11])[C:5]1[CH:10]=[CH:9][CH:8]=[CH:7][CH:6]=1

参加物

5

反応条件

温度
5 °C

実験手順

30.2 g (0.2 mol) of N-hydroxymethylbenzamide were dissolved in 50 ml of tetrahydrofuran and cooled to 5° C. with stirring, then a solution of 11 g (0.1 mol) of diphosphorus trioxide (P2O3) in 20 ml of tetrahydrofuran was added dropwise at 5°-15° C. during the course of 30 minutes under a nitrogen atmosphere. The reaction solution obtained was then cooled to 2° C. for 10 minutes. Cooling was then omitted, the internal temperature rising to 35° C. The mixture was then heated to reflux for 2 hours; a clear solution was not formed in this case. It was then cooled. 4.5 g (0.25 mol) of water were then added dropwise at 30°-35° C. with cooling. The mixture was then heated to reflux for 1 hour, then cooled and additionally stirred and finally filtered with suction. 25 g of benzoylaminomethanephosphonic acid having a melting point of 175° to 178° C. were obtained. A further 5.5 g were isolated from the mother liquor. Altogether, 30.5 g (71% of theory) of product were thus obtained.

後処理

  1. customThe reaction solution obtained
  2. temperaturewas then cooled to 2° C. for 10 minutes
  3. temperatureCooling
  4. customrising to 35° C
  5. temperatureThe mixture was then heated
  6. temperatureto reflux for 2 hours
  7. customa clear solution was not formed in this case
  8. temperatureIt was then cooled
  9. temperaturewith cooling
  10. temperatureThe mixture was then heated
  11. temperatureto reflux for 1 hour
  12. temperaturecooled
  13. stirringadditionally stirred
  14. filtrationfinally filtered with suction

出典と根拠

ORDレコード
ord-693741de573a48d281972fc8a11187a3
出典データセット
uspto-grants-1992_10
特許番号
US05155257

関連ノート

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