Technology Process of 2,2,2-Trifluoro-1,1-diphenyl-ethanesulfonic acid (1S,2R,3R,5S,6R,7R)-6-(2,2,2-trifluoro-1,1-diphenyl-ethanesulfonyloxy)-4,8-dioxa-tricyclo[5.1.0.03,5]oct-2-yl ester
There total 7 articles about 2,2,2-Trifluoro-1,1-diphenyl-ethanesulfonic acid (1S,2R,3R,5S,6R,7R)-6-(2,2,2-trifluoro-1,1-diphenyl-ethanesulfonyloxy)-4,8-dioxa-tricyclo[5.1.0.03,5]oct-2-yl ester which
guide to synthetic route it.
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synthetic route:
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112882-03-8,112965-57-8
2,2,2-Trifluoro-1,1-diphenyl-ethanesulfinic acid (1S,2R,3R,5S,6R,7R)-6-(2,2,2-trifluoro-1,1-diphenyl-ethanesulfinyloxy)-4,8-dioxa-tricyclo[5.1.0.03,5]oct-2-yl ester
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112882-11-8
2,2,2-Trifluoro-1,1-diphenyl-ethanesulfonic acid (1S,2R,3R,5S,6R,7R)-6-(2,2,2-trifluoro-1,1-diphenyl-ethanesulfonyloxy)-4,8-dioxa-tricyclo[5.1.0.03,5]oct-2-yl ester
- Guidance literature:
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With
disodium hydrogenphosphate; trifluoroacetyl peroxide;
In
dichloromethane;
Ambient temperature;
DOI:10.1055/s-1987-28045
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112882-11-8
2,2,2-Trifluoro-1,1-diphenyl-ethanesulfonic acid (1S,2R,3R,5S,6R,7R)-6-(2,2,2-trifluoro-1,1-diphenyl-ethanesulfonyloxy)-4,8-dioxa-tricyclo[5.1.0.03,5]oct-2-yl ester
- Guidance literature:
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Multi-step reaction with 7 steps
1: 1.) Mg / 1.) ether, 2.) reflux, 1 h
2: 1.) NaH / 1.) ether, room temp., 1 h, 2.) room temp., 70 h
3: 96 percent / H2S, p-TsOH / various solvent(s) / 1 h / 60 °C
4: 96 percent / sulfuryl chloride / diethyl ether / 0.25 h / Ambient temperature
5: 100 percent / CF3CO3H / CH2Cl2 / 0 deg C, 1 h; room temp., 1 h
6: 61 percent / N-methylimidazole / 0 deg C to room temp.
7: 92 percent / CF3CO3H, Na2HPO4 / CH2Cl2 / Ambient temperature
With
1-methyl-1H-imidazole; disodium hydrogenphosphate; sulfuryl dichloride; trifluoroacetyl peroxide; hydrogen sulfide; sodium hydride; toluene-4-sulfonic acid; magnesium;
In
diethyl ether; dichloromethane;
DOI:10.1055/s-1987-28045
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112882-11-8
2,2,2-Trifluoro-1,1-diphenyl-ethanesulfonic acid (1S,2R,3R,5S,6R,7R)-6-(2,2,2-trifluoro-1,1-diphenyl-ethanesulfonyloxy)-4,8-dioxa-tricyclo[5.1.0.03,5]oct-2-yl ester
- Guidance literature:
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Multi-step reaction with 6 steps
1: 1.) NaH / 1.) ether, room temp., 1 h, 2.) room temp., 70 h
2: 96 percent / H2S, p-TsOH / various solvent(s) / 1 h / 60 °C
3: 96 percent / sulfuryl chloride / diethyl ether / 0.25 h / Ambient temperature
4: 100 percent / CF3CO3H / CH2Cl2 / 0 deg C, 1 h; room temp., 1 h
5: 61 percent / N-methylimidazole / 0 deg C to room temp.
6: 92 percent / CF3CO3H, Na2HPO4 / CH2Cl2 / Ambient temperature
With
1-methyl-1H-imidazole; disodium hydrogenphosphate; sulfuryl dichloride; trifluoroacetyl peroxide; hydrogen sulfide; sodium hydride; toluene-4-sulfonic acid;
In
diethyl ether; dichloromethane;
DOI:10.1055/s-1987-28045