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Benzyl 4-formylbenzoate → 4-[(Dimethoxy-phosphoryl)-hydroxy-methyl]-benzoic acid benzyl ester

HRID 1013481
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HRID 1013481 반응식
[CH2:1]([O:8][C:9](=[O:18])[C:10]1[CH:15]=[CH:14][C:13]([CH:16]=[O:17])=[CH:12][CH:11]=1)[C:2]1[CH:7]=[CH:6][CH:5]=[CH:4][CH:3]=1.[P:19]([O-:24])([O:22][CH3:23])[O:20][CH3:21]>C1COCC1.CCOC(C)=O>[CH2:1]([O:8][C:9](=[O:18])[C:10]1[CH:11]=[CH:12][C:13]([CH:16]([P:19]([O:22][CH3:23])([O:20][CH3:21])=[O:24])[OH:17])=[CH:14][CH:15]=1)[C:2]1[CH:3]=[CH:4][CH:5]=[CH:6][CH:7]=1
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

5

반응물 2

HCID 11528845Benzyl 4-formylbenzoateHCID 21884954Dimethylphosphite

생성물 1

HCID 579259274-[(Dimethoxy-phosphoryl)-hydroxy-methyl]-benzoic acid benzyl ester

시약·촉매·용매 2

HCID 8028Tetrahydrofuran용매HCID 8857Ethyl Acetate용매

실험 절차

A solution of 4-formyl-benzoic acid benzyl ester (0.50 g, 2.08 mmol) in THF (2.0 mL) was cooled to 0° C., then dimethyl phosphite (0.25 g, 2.29 mmol) and N,N,N′M′-tetramethyl-guanidine (0.02 g, 0.21 mmol) was added dropwise. The reaction mixture was warmed to ambient temperature. After stirring for 45 mins the reaction mixture was diluted with EtOAc and washed with 1N aqueous HCl (2×), brine, then dried (MgSO4) and concentrated in vacuo to give the title compound: MS: cal'd 351 (MH+), exp 351 (MH+)

후처리

  1. washwashed with 1N aqueous HCl (2×), brine
  2. dry with materialdried (MgSO4)
  3. concentrationconcentrated in vacuo

출처 및 근거

ORD 기록
ord-bb628ef23e384835835f26195091572d
출처 데이터셋
uspto-grants-2011_07
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US07981874B2

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