18-Crown-6 → Methyl 3-(3-cyanophenyl)prop-2-enoate

HRID 2184898

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HRID 2184898 반응식
P(=O)([O-])O[C:3]([CH2:13][C:14](F)(F)F)(CC(F)(F)F)[C:4]([O:6][CH3:7])=[O:5].C1OCCOCCOCCOCCOCCOC1.C[Si]([N-][Si](C)(C)C)(C)C.[K+].[C:48]([C:50]1[CH:51]=C([CH:55]=[CH:56][CH:57]=1)C=O)#[N:49]>C1COCC1.CCOC(C)=O.CCCCCC>[C:48]([C:50]1[CH:51]=[C:14]([CH:55]=[CH:56][CH:57]=1)[CH:13]=[CH:3][C:4]([O:6][CH3:7])=[O:5])#[N:49]

참가 물질

7

실험 절차

To a solution of bis(2,2,2-trifluoroethyl)(methoxycarbonylmethyl) phosphonate (1.00 g, 3.14 mmol) and 18-crown-6 (4.14 g, 15.7 mmol) in THF (50 mL) at −78 C, potassium bis(trimethylsilyl)amide (6.3 mL, 0.5 M in toluene, 3.15 mmol) was added dropwise. After the addition was completed, 3-cyanobenzaldehyde (0.412 g, 3.14 mmol) in THF (8 mL) was added. The mixture was stirred at −78 C for 30 min before it was quenched with aq. NH4Cl. Water and ether were added. Aqueous phase was separated, extracted with ether once more. The combined organic solutions were dried over Na2SO4, concentrated in vacuo to give a solid, which was purified by a silica gel column, first eluted with EtOAc/hexane (5/95), then with EtOAc/hexane (10/90) to give the titled compound (0.40 g) (yield: 68%). 1H NMR (CDCl3) 7.85 (s, 1H), 7.77 (d, 1H, J=8 Hz), 7.60 (d, 1H, J=8 Hz), 7.45 (t, 1H, J=8 Hz), 6.91 (d, 1H, J=12 Hz), 6.06 (d, 1H, J=12 Hz).

후처리

  1. additionAfter the addition
  2. customwas quenched with aq. NH4Cl
  3. additionWater and ether were added
  4. customAqueous phase was separated
  5. extractionextracted with ether once more
  6. dry with materialThe combined organic solutions were dried over Na2SO4
  7. concentrationconcentrated in vacuo
  8. customto give a solid, which
  9. customwas purified by a silica gel column
  10. washfirst eluted with EtOAc/hexane (5/95)

출처 및 근거

ORD 기록
ord-57f5192d728a4a3e8f6b70f7381216e3
출처 데이터셋
uspto-grants-2002_06
특허 번호
US06399627B1

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