4-[2-(4-chlorophenyl)-thiazol-4-ylmethyl]-2,2-bis(trifluoromethyl)-1,3-oxathiolan-5-one

Base Information

Chemical Name:4-[2-(4-chlorophenyl)-thiazol-4-ylmethyl]-2,2-bis(trifluoromethyl)-1,3-oxathiolan-5-one
CAS No.:1025965-57-4
Molecular Formula:C₁₅H₈ClF₆NO₂S₂
Molecular Weight:447.809
Hs Code.:

Synonyms:4-[2-(4-chlorophenyl)-thiazol-4-ylmethyl]-2,2-bis(trifluoromethyl)-1,3-oxathiolan-5-one

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Chemical Property of 4-[2-(4-chlorophenyl)-thiazol-4-ylmethyl]-2,2-bis(trifluoromethyl)-1,3-oxathiolan-5-one

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Technology Process of 4-[2-(4-chlorophenyl)-thiazol-4-ylmethyl]-2,2-bis(trifluoromethyl)-1,3-oxathiolan-5-one

There total 4 articles about 4-[2-(4-chlorophenyl)-thiazol-4-ylmethyl]-2,2-bis(trifluoromethyl)-1,3-oxathiolan-5-one which guide to synthetic route it. The literature collected by LookChem mainly comes from the sharing of users and the free literature resources found by Internet computing technology. We keep the original model of the professional version of literature to make it easier and faster for users to retrieve and use. At the same time, we analyze and calculate the most feasible synthesis route with the highest yield for your reference as below:

synthetic route:

Reference yield: 56.0%

: 2521-24-6
4-chlorothiobenzamide

: 599197-95-2
4-(3-bromo-2-oxopropyl)-2,2-bis(trifluoromethyl)-1,3-oxathiolan-5-one

: 1025965-57-4
4-[2-(4-chlorophenyl)-thiazol-4-ylmethyl]-2,2-bis(trifluoromethyl)-1,3-oxathiolan-5-one

Guidance literature:: 4-chlorothiobenzamide; 4-(3-bromo-2-oxopropyl)-2,2-bis(trifluoromethyl)-1,3-oxathiolan-5-one; In acetone;

With sodium hydrogencarbonate; In diethyl ether;
DOI:10.1002/jhet.5570400306

Reference yield:

: 170996-97-1
[2,2-bis(trifluoromethyl)-5-oxo-1,3-oxathiolan-4-yl]acetic acid

: 1025965-57-4
4-[2-(4-chlorophenyl)-thiazol-4-ylmethyl]-2,2-bis(trifluoromethyl)-1,3-oxathiolan-5-one

Guidance literature:: Multi-step reaction with 4 steps

1.1: 88 percent / thionyl chloride / 6 h / Heating

2.1: 93 percent / diethyl ether / 0.5 h / 0 °C

3.1: 82 percent / conc. HBr / tetrahydrofuran / -78 °C

4.1: acetone

4.2: 56 percent / NaHCO₃ / diethyl ether

With thionyl chloride; hydrogen bromide; In tetrahydrofuran; diethyl ether; acetone;
DOI:10.1002/jhet.5570400306

Reference yield:

: 170996-99-3
[2,2-bis(trifluoromethyl)-5-oxo-1,3-oxathiolan-4-yl]-acetyl chloride

: 1025965-57-4
4-[2-(4-chlorophenyl)-thiazol-4-ylmethyl]-2,2-bis(trifluoromethyl)-1,3-oxathiolan-5-one

Guidance literature:: Multi-step reaction with 3 steps

1.1: 93 percent / diethyl ether / 0.5 h / 0 °C

2.1: 82 percent / conc. HBr / tetrahydrofuran / -78 °C

3.1: acetone

3.2: 56 percent / NaHCO₃ / diethyl ether

With hydrogen bromide; In tetrahydrofuran; diethyl ether; acetone;
DOI:10.1002/jhet.5570400306