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Tetrahydrofuran → 4-(1,1-Dimethyl-4,4,4-trifluoro-2-butynyl)anisole

HRID 2269265
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HRID 2269265 반응식
[Li][CH2:2]CCC.[F:6][C:7]([F:13])([F:12])S([O-])(=O)=O.FC(F)(F)[S+]1[C:20]2C=C[CH:23]=[CH:24][C:19]=2[C:18]2[CH:25]=[CH:26][CH:27]=[CH:28][C:17]1=2.C1C[O:34][CH2:33]C1>>[CH3:2][C:19]([C:18]1[CH:17]=[CH:28][C:27]([O:34][CH3:33])=[CH:26][CH:25]=1)([CH3:20])[C:24]#[C:23][C:7]([F:13])([F:12])[F:6]
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참가 물질

4

반응물 3

HCID 8028TetrahydrofuranHCID 27775075-(Trifluoromethyl)dibenzothiophenium trifluoromethanesulfonateHCID 178418339Butyllithium

생성물 1

HCID 186775904-(1,1-Dimethyl-4,4,4-trifluoro-2-butynyl)anisole수율 13%

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온도
0 °C

실험 절차

To a stirred solution of Compound 56 (0.22 g, 1.26 mmol) in THF (8 ml) was added n-BuLi (1.69 M in hexane, 0.82 ml, 1.39 mmol) at −78° C. under N2, then warmed up to 0° C., and stirred for 1 h. S-(Trifluoromethyl)dibenzothiophenium trifluoromethane-sulfonate (1.01 g, 2.52 mmol) was added, and stirred for 3 h at 0° C. The mixture was quenched by the addition of NaHCO3 aq., and extracted with CH2Cl2. The combined organic layers were dried over MgSO4, filtered, and concentrated. This was purified by SiO2 chromatography to give Compound 57 (38 mg, 13%) as a colorless oil.

후처리

  1. stirringstirred for 3 h at 0° C
  2. customThe mixture was quenched by the addition of NaHCO3 aq.
  3. extractionextracted with CH2Cl2
  4. dry with materialThe combined organic layers were dried over MgSO4
  5. filtrationfiltered
  6. concentrationconcentrated
  7. customThis was purified by SiO2 chromatography

출처 및 근거

ORD 기록
ord-65b09b873966426fb341b59ac38de3fc
출처 데이터셋
uspto-grants-2001_12
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US06329396B1

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