3-Boc-2,2-dimethyloxazolidine-4-carboxaldehyde, (S)-(-)- → HCID 68839236, 화합물

HRID 660559

반응식

HRID 660559 반응식
[Br-].[CH2:2]([O:4][C:5]([C:7]1[CH:32]=[CH:31][CH:30]=[CH:29][C:8]=1[CH2:9][P+](C1C=CC=CC=1)(C1C=CC=CC=1)C1C=CC=CC=1)=[O:6])[CH3:3].C[Si]([N-][Si](C)(C)C)(C)C.[K+].[C:43]([O:47][C:48]([N:50]1[C@H:54]([CH:55]=O)[CH2:53][O:52][C:51]1([CH3:58])[CH3:57])=[O:49])([CH3:46])([CH3:45])[CH3:44]>C1(C)C=CC=CC=1>[C:43]([O:47][C:48]([N:50]1[C@H:54]([CH:55]=[CH:9][C:8]2[CH:29]=[CH:30][CH:31]=[CH:32][C:7]=2[C:5]([O:4][CH2:2][CH3:3])=[O:6])[CH2:53][O:52][C:51]1([CH3:57])[CH3:58])=[O:49])([CH3:46])([CH3:44])[CH3:45]

참가 물질

5

반응물 3

HCID 1798243-Boc-2,2-dimethyloxazolidine-4-carboxaldehyde, (S)-(-)-HCID 3251421Potassium bis(trimethylsilyl)amideHCID 19092713{[2-(Ethoxycarbonyl)phenyl]methyl}(triphenyl)phosphanium bromide

생성물 1

HCID 68839236HCID 68839236, 화합물

시약·촉매·용매 1

HCID 1140Toluene용매

실험 절차

To a suspension of (2-ethoxycarbonylbenzyl)-triphenylphosphonium bromide (9.0 g, 17.77 mmol) in toluene (100 mL) is added potassium bis(trimethylsilyl)amide (0.5M in toluene, 40 mL) followed by the addition of (S)-4-formyl-2,2-dimethyloxazolidine-3-carboxylic acid tert-butyl ester (3.4 g, 14.83 mmol) and the mixture is refluxed for 1 h. After cooling to RT, ice/water is added and the solution extracted with EtOAc. The organic layer is washed with brine, dried over MgSO4, filtered and concentrated. The crude material is purified by column chromatography to afford the title compound as a yellow oil: (M+1)+=376.

후처리

  1. temperaturethe mixture is refluxed for 1 h
  2. extractionthe solution extracted with EtOAc
  3. washThe organic layer is washed with brine
  4. dry with materialdried over MgSO4
  5. filtrationfiltered
  6. concentrationconcentrated
  7. customThe crude material is purified by column chromatography

출처 및 근거

ORD 기록
ord-4796e25e8e5a4414b94bcacc3d4b7926
출처 데이터셋
uspto-grants-2011_12
특허 번호
US08084448B2

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