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llms.txt · MCP 가이드개인정보처리방침 · 이용약관 · 지원v1.8.0
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Tetraethyl (phenoxymethylene)-bisphosphonate → (Phenoxymethylene)-bisphosphonic acid

HRID 569606
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인쇄 미리보기

반응식

HRID 569606 반응식
[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
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

3

반응물 1

HCID 54483224Tetraethyl (phenoxymethylene)-bisphosphonate

생성물 1

HCID 9816823(Phenoxymethylene)-bisphosphonic acid

시약·촉매·용매 1

HCID 313Hydrochloric Acid용매

실험 절차

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.

후처리

  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

출처 및 근거

ORD 기록
ord-fed28e7d18344f6e97ba7c2d9727c9ab
출처 데이터셋
uspto-grants-1988_03
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US04732998

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