Tetrahydrofuran → 5-Chloro-9-isopropylidene-1,4-dihydro-1,4-methano-naphthalene

HRID 39410

Reaktionsgleichung

Reaktionsgleichung von HRID 39410
Br[C:2]1[C:7](Cl)=[CH:6][CH:5]=[CH:4][C:3]=1[Cl:9].C([Mg]Cl)(C)C.O1CCCC1.[CH3:20][C:21]([CH3:27])=[C:22]1[CH:26]=[CH:25][CH:24]=[CH:23]1>C1(C)C=CC=CC=1>[Cl:9][C:3]1[CH:4]=[CH:5][CH:6]=[C:7]2[C:2]=1[CH:23]1[C:22](=[C:21]([CH3:27])[CH3:20])[CH:26]2[CH:25]=[CH:24]1

Komponenten

6

Versuchsvorschrift

A solution of 2-bromo-1,3-dichlorobenzene (22.59 g, 0.1 mol) in dry toluene (100 ml) under a nitrogen atmosphere was reacted at −8 to −15° C. with 2M isopropylmagnesium chloride in tetrahydrofuran (50 ml, 0.1 mol) for 1 hour. Subsequent addition of 6,6-dimethylfulvene (13.03 g, assay 97.8%, 0.12 mol) at 0° C. was followed by heating to reflux temperature for 10 hours. Aqueous work up with saturated aqueous ammonium chloride and ethyl acetate extraction followed by washings with brine and water and drying over sodium sulphate gave the crude material which was purified by chromatography on silica gel in hexane to give the desired product (19.03 g, assay 95.2% by g.l.c., 83.6% yield) as a yellow solid. This reaction is also disclosed in WO 2007/068417.

Aufarbeitung

  1. temperatureby heating
  2. temperatureto reflux temperature for 10 hours
  3. extractionAqueous work up with saturated aqueous ammonium chloride and ethyl acetate extraction
  4. washfollowed by washings with brine and water
  5. dry with materialdrying over sodium sulphate
  6. customgave the crude material which
  7. customwas purified by chromatography on silica gel in hexane

Quellen und Nachweise

ORD-Eintrag
ord-0153af4bec6c4c0a81eca3ce9422b924
Quelldatensatz
uspto-grants-2013_09
Patentnummer
US08524915B2

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