Technology Process of Dimethylamino-(2,2,3-trimethyl-6-methylene-cyclohexyl)-acetonitrile
There total 6 articles about Dimethylamino-(2,2,3-trimethyl-6-methylene-cyclohexyl)-acetonitrile which
guide to synthetic route it.
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synthetic route:
- Guidance literature:
-
Multi-step reaction with 6 steps
1: 93 percent / H2 / Raney Ni / hexane / 3 h / 140 °C
2: 86 percent / CrO3, water, H2SO4 / acetone / 3 h / 20 °C
3: 1) 63 percent NaH; 2) HCOOEt, 12 percent aq. HCl / 1) mineral oil, toluene, 2 h, 100 deg C; 2 h, 60 deg C; 2) toluene, mineral oil, 12 h, RT
4: 97 percent / H3PO4 / 12 h / Ambient temperature
6: 1) methanesulfonyl chloride, NEt3; 2) Na2CO3 / 1) ether, 2 h, 10 deg C; 2) MeCN, 4 h, reflux
With
chromium(VI) oxide; hydrogenchloride; phosphoric acid; sulfuric acid; water; hydrogen; sodium hydride; sodium carbonate; methanesulfonyl chloride; triethylamine; formic acid ethyl ester;
nickel;
In
hexane; acetone;
- Guidance literature:
-
Multi-step reaction with 5 steps
1: 86 percent / CrO3, water, H2SO4 / acetone / 3 h / 20 °C
2: 1) 63 percent NaH; 2) HCOOEt, 12 percent aq. HCl / 1) mineral oil, toluene, 2 h, 100 deg C; 2 h, 60 deg C; 2) toluene, mineral oil, 12 h, RT
3: 97 percent / H3PO4 / 12 h / Ambient temperature
5: 1) methanesulfonyl chloride, NEt3; 2) Na2CO3 / 1) ether, 2 h, 10 deg C; 2) MeCN, 4 h, reflux
With
chromium(VI) oxide; hydrogenchloride; phosphoric acid; sulfuric acid; water; sodium hydride; sodium carbonate; methanesulfonyl chloride; triethylamine; formic acid ethyl ester;
In
acetone;
- Guidance literature:
-
Multi-step reaction with 4 steps
1: 1) 63 percent NaH; 2) HCOOEt, 12 percent aq. HCl / 1) mineral oil, toluene, 2 h, 100 deg C; 2 h, 60 deg C; 2) toluene, mineral oil, 12 h, RT
2: 97 percent / H3PO4 / 12 h / Ambient temperature
4: 1) methanesulfonyl chloride, NEt3; 2) Na2CO3 / 1) ether, 2 h, 10 deg C; 2) MeCN, 4 h, reflux
With
hydrogenchloride; phosphoric acid; sodium hydride; sodium carbonate; methanesulfonyl chloride; triethylamine; formic acid ethyl ester;