Tri-o-tolylphosphine → diisopropyl (2S,3R)-2-hydroxy-3-{(2E)-3-[4-(trifluoromethoxy)phenyl]-2-propenyl}butanedioate

HRID 888230노트

반응식

HRID 888230 반응식
[CH2:1]([C@H:4]([C@H:11]([OH:18])[C:12]([O:14][CH:15]([CH3:17])[CH3:16])=[O:13])[C:5]([O:7][CH:8]([CH3:10])[CH3:9])=[O:6])[CH:2]=[CH2:3].Br[C:20]1[CH:25]=[CH:24][C:23]([O:26][C:27]([F:30])([F:29])[F:28])=[CH:22][CH:21]=1.C1(C)C=CC=CC=1P(C1C=CC=CC=1C)C1C=CC=CC=1C>CC#N.C([O-])(=O)C.[Pd+2].C([O-])(=O)C>[OH:18][C@@H:11]([C@@H:4]([CH2:1]/[CH:2]=[CH:3]/[C:20]1[CH:21]=[CH:22][C:23]([O:26][C:27]([F:28])([F:29])[F:30])=[CH:24][CH:25]=1)[C:5]([O:7][CH:8]([CH3:10])[CH3:9])=[O:6])[C:12]([O:14][CH:15]([CH3:17])[CH3:16])=[O:13]

참가 물질

6

반응물 3

HCID 80271Tri-o-tolylphosphineHCID 5210081-Bromo-4-(trifluoromethoxy)benzeneHCID 59875729diisopropyl (2R,3S)-2-allyl-3-hydroxybutanedioate2회

생성물 1

HCID 58488014diisopropyl (2S,3R)-2-hydroxy-3-{(2E)-3-[4-(trifluoromethoxy)phenyl]-2-propenyl}butanedioate수율 86.2%

시약·촉매·용매 2

HCID 167845palladium(II) acetate촉매HCID 6342Acetonitrile용매2회

반응 조건

온도
80 °C

실험 절차

To a solution of diisopropyl (2R,3S)-2-allyl-3-hydroxybutanedioate (Intermediate 2a, 5.0 g; 19.4 mmol; 1.0 eq.), TEA (6.23 mL; 46.5 mmol; 2.4 eq.) in CH3CN (50.0 mL) was added 1-bromo-4-(trifluoromethoxy)benzene (5.13 g; 21.3 mmol; 1.1 eq.). To this solution was added a sonicated mixture of tri-o-tolylphosphine (0.59 g; 1.94 mmol; 0.10 eq.) and palladium(II) acetate (43.46 mg; 0.19 mmol; 0.01 eq.) in CH3CN (4 mL). The reaction was stirred at 80° C. for 14 h, cooled to RT and the solvents were evaporated (rotavap). The residue was taken up in EtOAc and washed with an aqueous saturated solution of NH4Cl, an aqueous saturated solution of NaHCO3 and then with an aqueous saturated solution of NaCl and dried over MgSO4. Evaporation of the solvent gave an oil. Purification by chromatography (SiO2, gradient from 10/90 EtOAc/c-hex to 100/0 EtOAc/c-hex in 30 min.) gave a colorless oil (6.98 g, 86.2%). M+(ESI): 419.2; M−(ESI): 417.0.

후처리

  1. additionTo this solution was added
  2. temperaturecooled to RT
  3. customthe solvents were evaporated (rotavap)
  4. washwashed with an aqueous saturated solution of NH4Cl
  5. dry with materialan aqueous saturated solution of NaHCO3 and then with an aqueous saturated solution of NaCl and dried over MgSO4
  6. customEvaporation of the solvent
  7. customgave an oil
  8. customPurification by chromatography (SiO2, gradient from 10/90 EtOAc/c-hex to 100/0 EtOAc/c-hex in 30 min.)

출처 및 근거

ORD 기록
ord-79cc589773674b9790324246d32cd10e
출처 데이터셋
uspto-grants-2012_08
특허 번호
US08247437B2

반응 노트

불러오는 중…