Technology Process of 4-(1-amino-2,2,2-trifluoro-ethyl)-4-cyclopropylmethyl-cyclohexanol hydrochloride
There total 5 articles about 4-(1-amino-2,2,2-trifluoro-ethyl)-4-cyclopropylmethyl-cyclohexanol hydrochloride which
guide to synthetic route it.
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synthetic route:
- Guidance literature:
-
With
hydrogenchloride;
In
water; isopropyl alcohol;
at 20 - 50 ℃;
- Guidance literature:
-
Multi-step reaction with 6 steps
1.1: tetrahydrofuran; diisobutylaluminium hydride / toluene / -78 - 0 °C
2.1: titanium(IV) tetraethanolate / tetrahydrofuran / 21 h / 20 °C / Reflux
3.1: tetramethylammonium fluoride / tetrahydrofuran / -40 - 0 °C
4.1: acetic acid / 0.17 h / 130 °C / Microwave irradiation
4.2: 0.5 h / 20 °C
5.1: sodium tetrahydroborate / ethanol / 0 °C
6.1: hydrogenchloride / water; isopropyl alcohol / 20 - 50 °C
With
tetrahydrofuran; hydrogenchloride; titanium(IV) tetraethanolate; sodium tetrahydroborate; tetramethylammonium fluoride; diisobutylaluminium hydride; acetic acid;
In
tetrahydrofuran; ethanol; water; isopropyl alcohol; toluene;
- Guidance literature:
-
Multi-step reaction with 5 steps
1.1: titanium(IV) tetraethanolate / tetrahydrofuran / 21 h / 20 °C / Reflux
2.1: tetramethylammonium fluoride / tetrahydrofuran / -40 - 0 °C
3.1: acetic acid / 0.17 h / 130 °C / Microwave irradiation
3.2: 0.5 h / 20 °C
4.1: sodium tetrahydroborate / ethanol / 0 °C
5.1: hydrogenchloride / water; isopropyl alcohol / 20 - 50 °C
With
hydrogenchloride; titanium(IV) tetraethanolate; sodium tetrahydroborate; tetramethylammonium fluoride; acetic acid;
In
tetrahydrofuran; ethanol; water; isopropyl alcohol;