4-Bromothioanisole → Dimethyl 2-thioanisylterepthalate

HRID 1493852

Reaktionsgleichung

Reaktionsgleichung von HRID 1493852
Br[C:2]1[CH:7]=[CH:6][C:5]([S:8][CH3:9])=[CH:4][CH:3]=1.[Li][C:11](C)(C)C.[CH3:15][O:16][C:17](=[O:29])[C:18]1[CH:27]=[CH:26][C:21]([C:22]([O:24][CH3:25])=[O:23])=[CH:20][C:19]=1Br>O1CCCC1.[Cl-].[Cl-].[Zn+2].Cl[Ni](Cl)([P](C1C=CC=CC=1)(C1C=CC=CC=1)C1C=CC=CC=1)[P](C1C=CC=CC=1)(C1C=CC=CC=1)C1C=CC=CC=1>[CH3:11][C:2]1[CH:7]=[CH:6][C:5]([S:8][CH3:9])=[CH:4][C:3]=1[C:19]1[CH:20]=[C:21]([C:22]([O:24][CH3:25])=[O:23])[CH:26]=[CH:27][C:18]=1[C:17]([O:16][CH3:15])=[O:29]

Komponenten

7

Edukt 3

HCID 660374-BromothioanisoleHCID 87741Dimethyl 2-bromoterephthalateHCID 178418306HCID 178418306, Verbindung

Produkt 1

HCID 86744855Dimethyl 2-thioanisylterepthalate

Reagenzien, Katalysatoren, Lösungsmittel 3

HCID 3007855ZincchlorideKatalysatorHCID 178418751HCID 178418751, VerbindungKatalysatorHCID 8028TetrahydrofuranLösungsmittel2×

Versuchsvorschrift

4-Bromothioanisole (7.1 g) was dissolved in tetrahydrofuran (23 ml). To this solution at -78° C. under nitrogen was added over a ten minute period 1.7M tBuLi (48 ml). After 45 minutes at room temperature, 1M ZnCl2 (41 ml) was added dropwise over a ten minute period. After one half hour at room temperature, bis(triphenylphosphine)nickel(II) chloride (1.4 g) was added followed by dimethyl-2-bromoterepthalate (4.67 g) in tetrahydrofuran (47 ml). The reaction mixture was stirred at room temperature for 45 minutes. The THF was removed under reduced pressure. The residue was treated with ethyl acetate and 1N HCl and the layers separated. The organic phase was washed with water, brine, dried over magnesium sulfate and evaporated gave the crude product. Chromatography on silica gel using 15% ethyl acetate/hexanes gave the desired product (3.92 g).

Aufarbeitung

  1. waitAfter one half hour at room temperature
  2. customThe THF was removed under reduced pressure
  3. additionThe residue was treated with ethyl acetate and 1N HCl
  4. customthe layers separated
  5. washThe organic phase was washed with water, brine
  6. dry with materialdried over magnesium sulfate
  7. customevaporated
  8. customgave the crude product

Quellen und Nachweise

ORD-Eintrag
ord-34d2e9b246ad404a807df43f1ee17ec8
Quelldatensatz
uspto-grants-1991_06
Patentnummer
US05025007

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