Reaktion #2446099

ord-86167dd938714e4abe834d90aee04245

Reaktionsgleichung

ClCCl
dichloromethane
Oc1cccc2ccccc12
1-naphthol
CCN(CC)CC
triethyl amine
Oc1cccc2ccccc12
naphthol
C=C(C)C(=O)Cl
methacryloyl chloride
C=C(C)C(=O)Oc1cccc2ccccc12
naphthalen-1-yl methacrylate
Ausbeute 90.0%

Lösungsmittel

Reaktionsbedingungen

Temperatur
-5°CELSIUS
Detaillierte Bedingungen
See reaction.notes.procedure_details.

Aufarbeitung

  1. 1
    TrocknenAn oven dried 250 mL 2 neck round bottom flask
  2. 2
    Sonstigefitted with a dropping funnel and guard tube under inert atmosphere
  3. 3
    workup.ADDITIONwas added slowly over a period of 15 min at −5° C
  4. 4
    Temperaturto warm to room temperature
  5. 5
    workup.STIRRINGstirred for another 2 h at room temperature
  6. 6
    SonstigeReaction
  7. 7
    SonstigeReaction mixture
  8. 8
    workup.ADDITIONwas poured into a 500 mL
  9. 9
    Sonstigeseparating funnel
  10. 10
    Waschenthe organic layer was washed with water and aq. Na2CO3 The organic layer
  11. 11
    Waschenwere again washed with water
  12. 12
    Trocknendried over anhydrous Na2SO4
  13. 13
    SonstigeDCM was removed under reduced pressure

Vorschrift

An oven dried 250 mL 2 neck round bottom flask fitted with a dropping funnel and guard tube under inert atmosphere was charged with 100 mL of dry dichloromethane, 1-naphthol (1) (5.0 g, 34.6 mmol) and triethyl amine (7.0 g, 70.0 mmol). The flask was cooled to −5° C. (ice & water bath), methacryloyl chloride (2) (5.4 g, 52.0 mmol) was added slowly over a period of 15 min at −5° C. The reaction was stirred for 2 h at −5° C. and allow to warm to room temperature and stirred for another 2 h at room temperature. Reaction was monitored by TLC (until naphthol was absent). Reaction mixture was poured into a 500 mL separating funnel and the organic layer was washed with water and aq. Na2CO3 The organic layer were again washed with water and dried over anhydrous Na2SO4. DCM was removed under reduced pressure and the product was a viscous oil (compound 3) (6.61 g, yield 90%).

Quelle

DOI: 10.6084/m9.figshare.5104873.v1Patent: US08685616B2uspto-grants-2014_04