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Ammonium Acetate → methyl 4-[(E)-1-{4-[[di(tert-butoxy)phosphoryl](difluoro)methyl]benzyl}-1-(4-fluorobenzoyl)-4-phenyl-3 butenyl]benzoate

HRID 1371017
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HRID 1371017 반응식
[F:1][C:2]1[CH:29]=[CH:28][C:5]([C:6]([CH:8]([C:18]2[CH:27]=[CH:26][C:21]([C:22]([O:24][CH3:25])=[O:23])=[CH:20][CH:19]=2)[CH2:9]/[CH:10]=[CH:11]/[C:12]2[CH:17]=[CH:16][CH:15]=[CH:14][CH:13]=2)=[O:7])=[CH:4][CH:3]=1.CC(C)([O-])C.[K+].Br[CH2:37][C:38]1[CH:43]=[CH:42][C:41]([C:44]([P:47](=[O:58])([O:53][C:54]([CH3:57])([CH3:56])[CH3:55])[O:48][C:49]([CH3:52])([CH3:51])[CH3:50])([F:46])[F:45])=[CH:40][CH:39]=1.C([O-])(=O)C.[NH4+]>[I-].C([N+](CCCC)(CCCC)CCCC)CCC.C1COCC1>[C:54]([O:53][P:47]([C:44]([F:46])([F:45])[C:41]1[CH:42]=[CH:43][C:38]([CH2:37][C:8]([C:18]2[CH:19]=[CH:20][C:21]([C:22]([O:24][CH3:25])=[O:23])=[CH:26][CH:27]=2)([C:6](=[O:7])[C:5]2[CH:28]=[CH:29][C:2]([F:1])=[CH:3][CH:4]=2)[CH2:9]/[CH:10]=[CH:11]/[C:12]2[CH:17]=[CH:16][CH:15]=[CH:14][CH:13]=2)=[CH:39][CH:40]=1)([O:48][C:49]([CH3:52])([CH3:51])[CH3:50])=[O:58])([CH3:55])([CH3:56])[CH3:57]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

7

반응물 4

HCID 517165Ammonium AcetateHCID 15922636Di(tert-butyl) [4-(bromomethyl)phenyl](difluoro)methylphosphonateHCID 18510204methyl 4-[(E)-1-(4-fluorobenzoyl)-4-phenyl-3-butenyl]benzoateHCID 23665647Potassium tert-butoxide

생성물 1

HCID 86585140methyl 4-[(E)-1-{4-[[di(tert-butoxy)phosphoryl](difluoro)methyl]benzyl}-1-(4-fluorobenzoyl)-4-phenyl-3 butenyl]benzoate

시약·촉매·용매 2

HCID 67553Tetrabutylammonium Iodide촉매HCID 8028Tetrahydrofuran용매3회

실험 절차

To a solution of methyl 4-[(E)-1-(4-fluorobenzoyl)-4-phenyl-3-butenyl]benzoate (racemate) (0.430 g, 1.10 mmol), 18 crown 6 (0.236 g) and a catalytic amount of tetrabutylammonium iodide in THF (5 ml) degassed at −78° C. was added potassium tert-butoxide 1 M in THF (1.1 ml, 1.10 mmol). After a period of 0.5 h, a solution of di(tert-butyl) [4-(bromomethyl)phenyl](difluoro)methylphosphonate (0.46 g, 1.11 mmol) in THF (5 ml) was added to the reaction mixture, and the reaction mixture was then stirred at room temperature for 1 hour. Saturated ammonium acetate solution (20 ml) was added and the mixture was extracted with ethyl acetate (20 ml). The organic phase was washed with brine and dried over sodium sulfate, filtered and evaporated to dryness. The residue was purified by flash chromatography using hexane/ethyl acetate 15% containing 1% triethylamine giving 0.39 g of the title compound.

후처리

  1. extractionthe mixture was extracted with ethyl acetate (20 ml)
  2. washThe organic phase was washed with brine
  3. dry with materialdried over sodium sulfate
  4. filtrationfiltered
  5. customevaporated to dryness
  6. customThe residue was purified by flash chromatography
  7. additioncontaining 1% triethylamine giving 0.39 g of the title compound

출처 및 근거

ORD 기록
ord-3261b524a3b347ea9edfab902c8d489d
출처 데이터셋
uspto-grants-2003_06
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US06583126B2

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