3-(3-chloro-4-methoxy-5-trifluoromethylbenzoyl)-2,3-dihydro-1,3-benzothiazole

Base Information

Chemical Name:3-(3-chloro-4-methoxy-5-trifluoromethylbenzoyl)-2,3-dihydro-1,3-benzothiazole
CAS No.:1285574-92-6
Molecular Formula:C₁₆H₁₁ClF₃NO₂S
Molecular Weight:373.783
Hs Code.:

Synonyms:3-(3-chloro-4-methoxy-5-trifluoromethylbenzoyl)-2,3-dihydro-1,3-benzothiazole

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Chemical Property of 3-(3-chloro-4-methoxy-5-trifluoromethylbenzoyl)-2,3-dihydro-1,3-benzothiazole

Chemical Property:

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Technology Process of 3-(3-chloro-4-methoxy-5-trifluoromethylbenzoyl)-2,3-dihydro-1,3-benzothiazole

There total 11 articles about 3-(3-chloro-4-methoxy-5-trifluoromethylbenzoyl)-2,3-dihydro-1,3-benzothiazole 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:

: 4433-52-7
2,3-dihydro-benzothiazole

: 1285574-91-5
3-chloro-4-methoxy-5-trifluoromethylbenzoyl chloride

: 1285574-92-6
3-(3-chloro-4-methoxy-5-trifluoromethylbenzoyl)-2,3-dihydro-1,3-benzothiazole

Guidance literature:: With triethylamine; In chloroform; at 20 ℃; for 1h;

Reference yield:

: 1272528-86-5
3-chloro-4-methoxy-5-trifluoromethylbenzoic acid

: 1285574-92-6
3-(3-chloro-4-methoxy-5-trifluoromethylbenzoyl)-2,3-dihydro-1,3-benzothiazole

Guidance literature:: Multi-step reaction with 2 steps

1: thionyl chloride / N,N-dimethyl-formamide / toluene / 16 h / 60 °C

2: triethylamine / chloroform / 1 h / 20 °C

With thionyl chloride; triethylamine; N,N-dimethyl-formamide; In chloroform; toluene;

Reference yield:

: 115933-50-1
methyl 4-hydroxy-3-(trifluoromethyl)benzoate

: 1285574-92-6
3-(3-chloro-4-methoxy-5-trifluoromethylbenzoyl)-2,3-dihydro-1,3-benzothiazole

Guidance literature:: Multi-step reaction with 5 steps

1: N-chloro-succinimide; trifluorormethanesulfonic acid / chloroform / 16 h / 20 °C

2: potassium carbonate / N,N-dimethyl-formamide / 2 h / 20 °C

3: lithium hydroxide monohydrate; water / tetrahydrofuran / 2 h / 20 °C

4: thionyl chloride / N,N-dimethyl-formamide / toluene / 16 h / 60 °C

5: triethylamine / chloroform / 1 h / 20 °C

With N-chloro-succinimide; thionyl chloride; lithium hydroxide monohydrate; trifluorormethanesulfonic acid; water; potassium carbonate; triethylamine; N,N-dimethyl-formamide; In tetrahydrofuran; chloroform; N,N-dimethyl-formamide; toluene;