Triphenylphosphine → Methyl 5-(2-benzyloxy-ethoxy)-2-nitro-benzoate
반응식
[OH:1][C:2]1[CH:3]=[CH:4][C:5]([N+:12]([O-:14])=[O:13])=[C:6]([CH:11]=1)[C:7]([O:9][CH3:10])=[O:8].C1(P(C2C=CC=CC=2)C2C=CC=CC=2)C=CC=CC=1.[CH2:34]([O:41][CH2:42][CH2:43]O)[C:35]1[CH:40]=[CH:39][CH:38]=[CH:37][CH:36]=1.CCOC(/N=N/C(OCC)=O)=O>O1CCCC1>[CH2:34]([O:41][CH2:42][CH2:43][O:1][C:2]1[CH:3]=[CH:4][C:5]([N+:12]([O-:14])=[O:13])=[C:6]([CH:11]=1)[C:7]([O:9][CH3:10])=[O:8])[C:35]1[CH:40]=[CH:39][CH:38]=[CH:37][CH:36]=1참가 물질
실험 절차
To a solution of methyl 5-hydroxy-2-nitro-benzoate (7.97 g, 40.43 mmol), triphenylphosphine (12.73 g, 48.53 mmol), and 2-benzyloxyethanol (5.86 ml, 41.24 mmol) in tetrahydofuran (100 ml) was added DEAD (8.04 ml, 95%, 48.51 mmol) dropwise. After addition of the DEAD, the reaction was stirred under nitrogen for 18 h. The solvent was evaporated, benzene was added, and the triphenylphosphine oxide was filtered off. The solid was washed with some benzene, and the filtrate evaporated. The yellow oil was dissolved in minimal benzene, and chromatographed on silica gel eluting with 25% ethyl acetate/hexanes to give methyl 5-(2-benzyloxy-ethoxy)-2-nitro-benzoate (12.47 g, 93%) as a light yellow oil. Analysis calculated for C17H17NO6 : C, 61.63; H, 5.17; N, 4.23. Found: C, 61.46; H, 5.02; N, 4.28.
후처리
- customThe solvent was evaporated
- additionbenzene was added
- filtrationthe triphenylphosphine oxide was filtered off
- washThe solid was washed with some benzene
- customthe filtrate evaporated
- dissolutionThe yellow oil was dissolved in minimal benzene
- customchromatographed on silica gel eluting with 25% ethyl acetate/hexanes
출처 및 근거
- ORD 기록
- ord-ac4f6ec9b9d94a3390bbbd2e71cdb15d
- 출처 데이터셋
- uspto-grants-2000_09
- 특허 번호
- US06124323
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