Technology Process of 3-ethoxy-1-phenyl-4H-imidazo<5,1-c><1,4>benzoxazine
There total 5 articles about 3-ethoxy-1-phenyl-4H-imidazo<5,1-c><1,4>benzoxazine which
guide to synthetic route it.
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synthetic route:
- Guidance literature:
-
Multi-step reaction with 4 steps
1: 80 percent / ethyldiisopropylamine / diethyl ether / 2 h / 20 °C
2: 65 percent / p-toluenesulphonic acid (p-TSA) / toluene / 75 °C
3: 95 percent / BF3 etherate / diethyl ether / 24 h / 20 °C
4: 1.) HCl gas, 2.) triethylamine / 1.) 0 deg C, 48 h, 2.) 48 h
With
hydrogenchloride; boron trifluoride diethyl etherate; toluene-4-sulfonic acid; triethylamine; N-ethyl-N,N-diisopropylamine;
In
diethyl ether; toluene;
DOI:10.3987/R-1986-12-3483
- Guidance literature:
-
Multi-step reaction with 4 steps
1: 80 percent / ethyldiisopropylamine / diethyl ether / 2 h / 20 °C
2: 65 percent / p-toluenesulphonic acid (p-TSA) / toluene / 75 °C
3: 95 percent / BF3 etherate / diethyl ether / 24 h / 20 °C
4: 1.) HCl gas, 2.) triethylamine / 1.) 0 deg C, 48 h, 2.) 48 h
With
hydrogenchloride; boron trifluoride diethyl etherate; toluene-4-sulfonic acid; triethylamine; N-ethyl-N,N-diisopropylamine;
In
diethyl ether; toluene;
DOI:10.3987/R-1986-12-3483
- Guidance literature:
-
Multi-step reaction with 2 steps
1: 95 percent / BF3 etherate / diethyl ether / 24 h / 20 °C
2: 1.) HCl gas, 2.) triethylamine / 1.) 0 deg C, 48 h, 2.) 48 h
With
hydrogenchloride; boron trifluoride diethyl etherate; triethylamine;
In
diethyl ether;
DOI:10.3987/R-1986-12-3483