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Potassium Carbonate → methyl (5E,8S)-8-[(tert-butoxycarbonyl)amino]-7-oxo-9-phenyl-non-5-enoate

HRID 638833
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HRID 638833 반응식
O=[CH:2][CH2:3][CH2:4][CH2:5][C:6]([O:8][CH3:9])=[O:7].[C:10]([O:14][C:15]([NH:17][C@@H:18]([CH2:28][C:29]1[CH:34]=[CH:33][CH:32]=[CH:31][CH:30]=1)[C:19](=[O:27])[CH2:20]P(=O)(OC)OC)=[O:16])([CH3:13])([CH3:12])[CH3:11].C([O-])([O-])=O.[K+].[K+]>C(O)C>[C:10]([O:14][C:15]([NH:17][C@@H:18]([CH2:28][C:29]1[CH:30]=[CH:31][CH:32]=[CH:33][CH:34]=1)[C:19](=[O:27])/[CH:20]=[CH:2]/[CH2:3][CH2:4][CH2:5][C:6]([O:8][CH3:9])=[O:7])=[O:16])([CH3:11])([CH3:12])[CH3:13]
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참가 물질

5

반응물 3

HCID 11430Potassium CarbonateHCID 554053Pentanoic acid, 5-oxo-, methyl esterHCID 7021151Dimethyl((3S)-4-phenyl-3-(Boc-amino)-2-oxobutyl)phosphonate

생성물 1

HCID 86614843methyl (5E,8S)-8-[(tert-butoxycarbonyl)amino]-7-oxo-9-phenyl-non-5-enoate수율 79%

시약·촉매·용매 1

HCID 702Ethanol용매

실험 절차

A solution of aldehyde (methyl 5-oxopentanoate) (1) (3.0 g, 23.1 mmol), in absolute ethanol (100 mL) is added, under stirring, to a solution of dimethyl (3S)-3-[(tert-butoxycarbonyl)amino]-2-oxo-4-phenylbutyl-phosphonate (2) (8.58 g, 23.1 mmol) and K2CO3 (3.2 g, 23.1 mmol), dried at 75° C. for 12 hours, in absolute ethanol (200 mL). The mixture is then stirred at room temperature for 16 hours, the solid residue is filtered off and the solution neutralised with glacial acetic acid. The solvent is removed under reduced pressure and the residue partitioned between ethyl acetate and a saturated solution of NaHCO3. The aqueous phase is extracted with ethyl acetate (2×50 mL) and the pooled organic phases are washed with a saturated NaCl solution and dried over anhydrous Na2SO4. The solvent is removed by distilling under reduced pressure and the product purified by means of flash chromatography on a silica gel column by using a 1:1 mixture of ethyl ether and petroleum ether as eluant. 6.8 g (79%) of a colourless oil are obtained.

후처리

  1. dry with materialdried at 75° C. for 12 hours, in absolute ethanol (200 mL)
  2. filtrationthe solid residue is filtered off
  3. customThe solvent is removed under reduced pressure
  4. customthe residue partitioned between ethyl acetate
  5. extractionThe aqueous phase is extracted with ethyl acetate (2×50 mL)
  6. washthe pooled organic phases are washed with a saturated NaCl solution
  7. dry with materialdried over anhydrous Na2SO4
  8. customThe solvent is removed
  9. distillationby distilling under reduced pressure
  10. customthe product purified by means of flash chromatography on a silica gel column
  11. additiona 1:1 mixture of ethyl ether and petroleum ether as eluant

출처 및 근거

ORD 기록
ord-2458a338e99d4e979d7641fbbd5f49af
출처 데이터셋
uspto-grants-2010_04
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US07691818B2

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