Reaktion #49007

ord-da442fe9c3494a84b96c52bc1aad841c

Reaktionsgleichung

CC(C)OC(=O)N=NC(=O)OC(C)C
Diisopropyl azodicarboxylate
c1ccc(P(c2ccccc2)c2ccccc2)cc1
triphenylphosphine
O=C1c2ccccc2C(=O)N1O
N-hydroxyphthalimide
CSCCCO
3-Methylsulfanyl-propan-1-ol
CSCCCON1C(=O)c2ccccc2C1=O
2-(3-methylsulfanyl-propoxy)-isoindole-1,3-dione
Ausbeute 65.4%

Lösungsmittel

Reaktionsbedingungen

Detaillierte Bedingungen
See reaction.notes.procedure_details.

Aufarbeitung

  1. 1
    workup.DISSOLUTIONdissolved
  2. 2
    Temperaturwith cooling the reaction vessel in an ice-bath under nitrogen atmosphere
  3. 3
    workup.STIRRINGstirred for 5 hours
  4. 4
    SonstigeAfter completion of the reaction
  5. 5
    Einengenthe reaction mixture was concentrated under reduced pressure
  6. 6
    Sonstigetriturated with diethyl ether:hexane (1:1, about 100 ml)
  7. 7
    Sonstigeto precipitate triphenylphosphine oxide as a white solid, which
  8. 8
    Filtrationwas filtered off
  9. 9
    EinengenThe filtrate was concentrated under reduced pressure
  10. 10
    Sonstigeto give a yellow oily residue
  11. 11
    SonstigeThe resultant yellow oil was purified by silica gel flash chromatography (BW300, Fuji Silysia Chemical, 20% ethyl acetate/hexane as an eluent)

Vorschrift

3-Methylsulfanyl-propan-1-ol (4.133 g, 38.92 mmol) was dissolved in THF (anhydrous, 100 mL). To this solution, triphenylphosphine (10.2 g, 38.92 mmol) and N-hydroxyphthalimide (6.4 mg, 38.92 mmol) were added and dissolved with stirring. Diisopropyl azodicarboxylate (8.5 mL, 42.812 mmol) was added dropwise thereto with cooling the reaction vessel in an ice-bath under nitrogen atmosphere. The reaction mixture was warmed to room temperature, and stirred for 5 hours. After completion of the reaction, the reaction mixture was concentrated under reduced pressure, and triturated with diethyl ether:hexane (1:1, about 100 ml) to precipitate triphenylphosphine oxide as a white solid, which was filtered off. The filtrate was concentrated under reduced pressure to give a yellow oily residue. The resultant yellow oil was purified by silica gel flash chromatography (BW300, Fuji Silysia Chemical, 20% ethyl acetate/hexane as an eluent) to give 2-(3-methylsulfanyl-propoxy)-isoindole-1,3-dione (6.4 g, 65%).

Quelle

DOI: 10.6084/m9.figshare.5104873.v1Patent: US07745663B2uspto-grants-2010_06