(2-Chloro-phenyl)-(2,2-dioxo-2,3-dihydro-2λ⁶-benzo[c]isothiazol-1-yl)-methanone

Base Information

Chemical Name:(2-Chloro-phenyl)-(2,2-dioxo-2,3-dihydro-2λ⁶-benzo[c]isothiazol-1-yl)-methanone
CAS No.:111249-12-8
Molecular Formula:C₁₄H₁₀ClNO₃S
Molecular Weight:307.757
Hs Code.:

(2-Chloro-phenyl)-(2,2-dioxo-2,3-dihydro-2λ<sup>6</sup>-benzo[c]isothiazol-1-yl)-methanone

Synonyms:(2-Chloro-phenyl)-(2,2-dioxo-2,3-dihydro-2λ⁶-benzo[c]isothiazol-1-yl)-methanone

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Chemical Property of (2-Chloro-phenyl)-(2,2-dioxo-2,3-dihydro-2λ⁶-benzo[c]isothiazol-1-yl)-methanone

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Technology Process of (2-Chloro-phenyl)-(2,2-dioxo-2,3-dihydro-2λ⁶-benzo[c]isothiazol-1-yl)-methanone

There total 3 articles about (2-Chloro-phenyl)-(2,2-dioxo-2,3-dihydro-2λ⁶-benzo[c]isothiazol-1-yl)-methanone 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: 75.0%

: 609-65-4
o-chlorobenzoyl chloride

: 111248-89-6
1,3-dihydro-2,1-benzisothiazole 2,2-dioxide

: 111249-12-8
(2-Chloro-phenyl)-(2,2-dioxo-2,3-dihydro-2λ⁶-benzo[c]isothiazol-1-yl)-methanone

Guidance literature:: With pyridine; at 0 ℃; for 3h;

Reference yield:

: 89665-79-2
(2-chlorophenyl)-methanesulfonamide

: 111249-12-8
(2-Chloro-phenyl)-(2,2-dioxo-2,3-dihydro-2λ⁶-benzo[c]isothiazol-1-yl)-methanone

Guidance literature:: Multi-step reaction with 2 steps

1: 62 percent / potassium carbonate, copper-bronze powder / various solvent(s) / 3 h / 180 °C

2: 75 percent / pyridine / 3 h / 0 °C

With pyridine; copper; potassium carbonate; In various solvent(s);

Reference yield:

: 111249-29-7
2-aminobenzylsulfonic acid sodium salt

: 111249-12-8
(2-Chloro-phenyl)-(2,2-dioxo-2,3-dihydro-2λ⁶-benzo[c]isothiazol-1-yl)-methanone

Guidance literature:: Multi-step reaction with 2 steps

1: 36 percent / POCl₃ / 3 h / 170 °C

2: 75 percent / pyridine / 3 h / 0 °C

With pyridine; trichlorophosphate;