Perfluorocyclopentene → 3,3'-(Perfluorocyclopent-1-ene-1,2-diyl)bis(2,5-bis(4-(tert-butyl)phenyl)thiophene)

HRID 708307

Reaktionsgleichung

Reaktionsgleichung von HRID 708307
Br[C:2]1[CH:6]=[C:5]([C:7]2[CH:12]=[CH:11][C:10]([C:13]([CH3:16])([CH3:15])[CH3:14])=[CH:9][CH:8]=2)[S:4][C:3]=1[C:17]1[CH:22]=[CH:21][C:20]([C:23]([CH3:26])([CH3:25])[CH3:24])=[CH:19][CH:18]=1.[F:27][C:28]1([F:39])[C:32](F)=[C:31](F)[C:30]([F:36])([F:35])[C:29]1([F:38])[F:37]>C1COCC1.CCOCC>[F:27][C:28]1([F:39])[C:29]([F:38])([F:37])[C:30]([F:36])([F:35])[C:31]([C:2]2[CH:6]=[C:5]([C:7]3[CH:8]=[CH:9][C:10]([C:13]([CH3:15])([CH3:14])[CH3:16])=[CH:11][CH:12]=3)[S:4][C:3]=2[C:17]2[CH:18]=[CH:19][C:20]([C:23]([CH3:24])([CH3:25])[CH3:26])=[CH:21][CH:22]=2)=[C:32]1[C:2]1[CH:6]=[C:5]([C:7]2[CH:12]=[CH:11][C:10]([C:13]([CH3:16])([CH3:15])[CH3:14])=[CH:9][CH:8]=2)[S:4][C:3]=1[C:17]1[CH:18]=[CH:19][C:20]([C:23]([CH3:26])([CH3:25])[CH3:24])=[CH:21][CH:22]=1

Komponenten

4

Edukt 2

HCID 11212PerfluorocyclopenteneHCID 679735833-Bromo-2,5-bis(4-(tert-butyl)phenyl)thiophene

Produkt 1

HCID 596155663,3'-(Perfluorocyclopent-1-ene-1,2-diyl)bis(2,5-bis(4-(tert-butyl)phenyl)thiophene)

Reagenzien, Katalysatoren, Lösungsmittel 1

HCID 21868444Ether tetrahydrofuranLösungsmittel

Versuchsvorschrift

A solution of (30) in anhydrous THF/ether cooled to −45° C. and treated with nBu—Li-(2.5 M in hexanes, 35 mL, 87 mmol) dropwise under a n argon atmosphere. The reaction mixture was stirred for a further 15 minutes followed by addition of octafluorocyclopentene (5.6 mL, 41.5 mmol) using a cooled gas tight syringe. The reaction was allowed to stir until the temperature reached −10° C., quenched by the addition of 10% HCl (50 mL). The aqueous layer was separated and extracted with ether. The organic phases were separated and pooled, dried over MgSO4, filtered and solvent removed by rotary evaporation. The crude product was stirred in MeOH for 3 hours, and the resulting precipitate filtered, dried and purified using flash chromatography (hexanes), affording 2 fractions—F1 was pure S006 (TLC), F2 contained S006 along with a fluorescent byproduct by TLC. F1, 5.35 g, 14.8%) and F2, 10.4 g (˜75% pure, 22%) as light yellow, powdery solids. 1H NMR (400 MHz, CDCl3) δ 7.37 (d, J=8.5 Hz, 4H), 7.30 (d, J=8.5 Hz, 4H), 7.05 (d, J=8.4 Hz, 4H), 6.92 (d, J=8.4 Hz, 4H), 6.13 (s, 2H), 1.34 (s, 18H), 0.91 (s, 18H).

Aufarbeitung

  1. stirringto stir until the temperature
  2. customreached −10° C.
  3. customquenched by the addition of 10% HCl (50 mL)
  4. customThe aqueous layer was separated
  5. extractionextracted with ether
  6. customThe organic phases were separated
  7. dry with materialdried over MgSO4
  8. filtrationfiltered
  9. customsolvent removed by rotary evaporation
  10. stirringThe crude product was stirred in MeOH for 3 hours
  11. filtrationthe resulting precipitate filtered
  12. customdried
  13. custompurified
  14. customaffording 2 fractions—F1

Quellen und Nachweise

ORD-Eintrag
ord-3a2835cccfc6448b9dc985acb4e8224f
Quelldatensatz
uspto-grants-2015_11
Patentnummer
US09176357B2

Verknüpfte Notizen

Wird geladen…