Technology Process of 2-ethyl-2-(3-phenylpropoxy)tetrahydro-2H-pyran
There total 6 articles about 2-ethyl-2-(3-phenylpropoxy)tetrahydro-2H-pyran which
guide to synthetic route it.
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synthetic route:
- Guidance literature:
-
With
(carbonyl)(chloro)(hydrido)tris(triphenylphosphine)ruthenium(II); diphenyl hydrogen phosphate;
In
toluene;
at 20 - 115 ℃;
for 23h;
Inert atmosphere;
DOI:10.1002/chem.201304270
- Guidance literature:
-
Multi-step reaction with 6 steps
1.1: 1H-imidazole / N,N-dimethyl-formamide / 20 °C / Inert atmosphere
2.1: oxalyl dichloride / dichloromethane; dimethyl sulfoxide / -78 - 20 °C / Inert atmosphere
2.2: 0.17 h / -78 °C
3.1: tetrahydrofuran / -78 - 20 °C / Inert atmosphere
4.1: sodium hexamethyldisilazane / toluene; 1,2-dimethoxyethane / 0.25 h / 0 - 50 °C / Inert atmosphere
4.2: 2 h
5.1: tetrabutyl ammonium fluoride / tetrahydrofuran / 6 h / 0 - 20 °C / Inert atmosphere
6.1: (carbonyl)(chloro)(hydrido)tris(triphenylphosphine)ruthenium(II); diphenyl hydrogen phosphate / toluene / 23 h / 20 - 115 °C / Inert atmosphere
With
1H-imidazole; (carbonyl)(chloro)(hydrido)tris(triphenylphosphine)ruthenium(II); oxalyl dichloride; diphenyl hydrogen phosphate; tetrabutyl ammonium fluoride; sodium hexamethyldisilazane;
In
tetrahydrofuran; 1,2-dimethoxyethane; dichloromethane; dimethyl sulfoxide; N,N-dimethyl-formamide; toluene;
DOI:10.1002/chem.201304270
- Guidance literature:
-
Multi-step reaction with 4 steps
1.1: tetrahydrofuran / -78 - 20 °C / Inert atmosphere
2.1: sodium hexamethyldisilazane / toluene; 1,2-dimethoxyethane / 0.25 h / 0 - 50 °C / Inert atmosphere
2.2: 2 h
3.1: tetrabutyl ammonium fluoride / tetrahydrofuran / 6 h / 0 - 20 °C / Inert atmosphere
4.1: (carbonyl)(chloro)(hydrido)tris(triphenylphosphine)ruthenium(II); diphenyl hydrogen phosphate / toluene / 23 h / 20 - 115 °C / Inert atmosphere
With
(carbonyl)(chloro)(hydrido)tris(triphenylphosphine)ruthenium(II); diphenyl hydrogen phosphate; tetrabutyl ammonium fluoride; sodium hexamethyldisilazane;
In
tetrahydrofuran; 1,2-dimethoxyethane; toluene;
DOI:10.1002/chem.201304270