反応 #595345

ord-6106c76da08c493da1bebffda33bcfaf

反応方程式

O=C(Cl)c1ccc(Cl)cc1
4-chlorobenzoyl chloride
COC(=O)CN=C=O
methyl isocyanatoacetate
CCN(CC)CC
triethylamine
COC(=O)c1ncoc1-c1ccc(Cl)cc1
Methyl 5-(4-chlorophenyl)-1,3-oxazole-4-carboxylate

溶媒

反応条件

詳細条件
See reaction.notes.procedure_details.

後処理

  1. 1
    その他The solvent is then removed on a rotary evaporator
  2. 2
    洗浄washed once with 5 ml of water
  3. 3
    乾燥The organic phase is dried over magnesium sulfate
  4. 4
    その他the solvent is removed on a rotary evaporator
  5. 5
    ろ過filtered off
  6. 6
    その他It is then recrystallized from about 10 ml of methanol
  7. 7
    その他This gives needle-shaped crystals which are dried in a drying cabinet at 50° C
  8. 8
    その他A further product fraction is obtained by reprecipitation
  9. 9
    その他after recrystallization

実験手順

1.40 g (8.00 mmol) of 4-chlorobenzoyl chloride, 1.00 g (10.09 mmol) of methyl isocyanatoacetate and 5.9 ml (42.39 mmol) of triethylamine are dissolved in 15 ml of dry THF and stirred at RT for 48 h. The solvent is then removed on a rotary evaporator. The residue is taken up in 20 ml of ethyl acetate and washed once with 5 ml of water. The organic phase is dried over magnesium sulfate and the solvent is removed on a rotary evaporator. The residue is suspended in 10 ml of cyclohexane and filtered off. It is then recrystallized from about 10 ml of methanol. This gives needle-shaped crystals which are dried in a drying cabinet at 50° C. A further product fraction is obtained by reprecipitation after recrystallization.

出典

DOI: 10.6084/m9.figshare.5104873.v1特許: US09095582B2uspto-grants-2015_08