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Diethyl [(4-benzoylphenyl)methyl]phosphonate → Phosphonic acid, [(4-benzoylphenyl)methyl]-

HRID 1728442
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HRID 1728442 반응식
C([O:3][P:4]([CH2:9][C:10]1[CH:15]=[CH:14][C:13]([C:16](=[O:23])[C:17]2[CH:22]=[CH:21][CH:20]=[CH:19][CH:18]=2)=[CH:12][CH:11]=1)(=[O:8])[O:5]CC)C>Cl>[C:16]([C:13]1[CH:14]=[CH:15][C:10]([CH2:9][P:4](=[O:3])([OH:5])[OH:8])=[CH:11][CH:12]=1)(=[O:23])[C:17]1[CH:18]=[CH:19][CH:20]=[CH:21][CH:22]=1
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참가 물질

3

반응물 1

HCID 56986843Diethyl [(4-benzoylphenyl)methyl]phosphonate

생성물 1

HCID 9795572Phosphonic acid, [(4-benzoylphenyl)methyl]-수율 26.4%

시약·촉매·용매 1

HCID 313Hydrochloric Acid용매

실험 절차

A mixture of 4.8 g of 4-benzoylbenzyl bromide and triethylphosphite was heated at 125° C. for 0.5 hours and cooled to room temperature. The resulting oil was purified by flash chromatography (70% ethyl acetate/hexanes) to afford 3.2 g of diethyl 4-benzoylbenzylphosphonic acid, as an oil. A mixture of 3.2 g (9.6 mmol) of diethyl 4-benzoylbenzylphosphonic acid and 40 ml of concentrated hydrochloric acid was refluxed for 7 hours and cooled to room temperature. The two phase mixture was partitioned between 125 ml of water and 400 ml of EtOAc, the EtOAc layer was dried over Na2SO4, filtered and evaporated to give 0.7 g of product; m.p. 172°-175° C.

후처리

  1. temperaturewas refluxed for 7 hours
  2. customThe two phase mixture was partitioned between 125 ml of water and 400 ml of EtOAc
  3. dry with materialthe EtOAc layer was dried over Na2SO4
  4. filtrationfiltered
  5. customevaporated

출처 및 근거

ORD 기록
ord-ee65471b454c41c88d762da6dd8843fa
출처 데이터셋
uspto-grants-1994_07
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US05326905

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