Trifluoroacetic acid → 4-[2-(4-Ethyl-4-oxido-1,4-azaphosphinan-1-yl)-2-oxoethyl]benzoic acid
반응식
[CH2:1]([P:3]1(=[O:25])[CH2:8][CH2:7][N:6]([C:9](=[O:24])[CH2:10][C:11]2[CH:23]=[CH:22][C:14]([C:15]([O:17]C(C)(C)C)=[O:16])=[CH:13][CH:12]=2)[CH2:5][CH2:4]1)[CH3:2].C(O)(C(F)(F)F)=O>C(Cl)Cl>[CH2:1]([P:3]1(=[O:25])[CH2:8][CH2:7][N:6]([C:9](=[O:24])[CH2:10][C:11]2[CH:23]=[CH:22][C:14]([C:15]([OH:17])=[O:16])=[CH:13][CH:12]=2)[CH2:5][CH2:4]1)[CH3:2]참가 물질
4
실험 절차
tert-Butyl 4-[2-(4-ethyl-4-oxido-1,4-azaphosphinan-1-yl)-2-oxoethyl]benzoate (270 mg, 0.739 mmol) was dissolved in CH2Cl2 (8 mL) and TFA (2 mL) and stirred at room temperature for 2 h. The solution was concentrated to dryness, redissolved in MeOH, and concentrated again to give the product as a colorless gum that was carried on without purification. MS: cal'd 310 (MH+), exp 310 (MH+).
후처리
- concentrationThe solution was concentrated to dryness
- dissolutionredissolved in MeOH
- concentrationconcentrated again
출처 및 근거
- ORD 기록
- ord-aae72704cdbb4ffdb00dfcd78b23778a
- 출처 데이터셋
- uspto-grants-2011_07
- 특허 번호
- US07981874B2
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