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Dibenzyl 3,4,5-trimethoxyphenylphosphonate → 3,4,5-Trimethoxyphenylphosphonic Acid

HRID 48082
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인쇄 미리보기

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HRID 48082 반응식
[CH3:1][O:2][C:3]1[CH:4]=[C:5]([P:13](=[O:30])([O:22]CC2C=CC=CC=2)[O:14]CC2C=CC=CC=2)[CH:6]=[C:7]([O:11][CH3:12])[C:8]=1[O:9][CH3:10]>C(OCC)(=O)C.[Pd]>[CH3:12][O:11][C:7]1[CH:6]=[C:5]([P:13](=[O:14])([OH:30])[OH:22])[CH:4]=[C:3]([O:2][CH3:1])[C:8]=1[O:9][CH3:10]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 1

HCID 54545930Dibenzyl 3,4,5-trimethoxyphenylphosphonate

생성물 1

HCID 206320103,4,5-Trimethoxyphenylphosphonic Acid

시약·촉매·용매 2

HCID 23938Palladium촉매HCID 8857Ethyl Acetate용매

실험 절차

To a solution of dibenzyl 3,4,5-trimethoxyphenylphosphonate 2 (1 mmol) in 30 mL of ethyl acetate is added 10% Pd on carbon (0.10 g). The mixture is stirred under an atmosphere of hydrogen for 16 hours. Mixture is filtered through celite and washed with methanol (3×10 mL). All washings and filtrate are combined and concentrated to give 3,4,5-trimethoxyphenylphosphonic acid 3.

후처리

  1. filtrationMixture is filtered through celite
  2. washwashed with methanol (3×10 mL)
  3. concentrationconcentrated

출처 및 근거

ORD 기록
ord-2dcfab923fbe41a4835acae0771e351a
출처 데이터셋
uspto-grants-2004_03
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US06702705B1

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