3-chloro-4-dimethoxymethyl-2-(1-oxothianylideneamino)benzoic acid methyl ester

Base Information

Chemical Name:3-chloro-4-dimethoxymethyl-2-(1-oxothianylideneamino)benzoic acid methyl ester
CAS No.:1207343-88-1
Molecular Formula:C₁₆H₂₂ClNO₅S
Molecular Weight:375.873
Hs Code.:

Synonyms:3-chloro-4-dimethoxymethyl-2-(1-oxothianylideneamino)benzoic acid methyl ester

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Chemical Property of 3-chloro-4-dimethoxymethyl-2-(1-oxothianylideneamino)benzoic acid methyl ester

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Technology Process of 3-chloro-4-dimethoxymethyl-2-(1-oxothianylideneamino)benzoic acid methyl ester

There total 6 articles about 3-chloro-4-dimethoxymethyl-2-(1-oxothianylideneamino)benzoic acid methyl ester 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: 100.0%

: 35188-35-3
1-iminohexahydro-1λ⁶-thiopyran-1-oxide

: 1207343-87-0
3-chloro-4-dimethoxymethyl-2-trifluoromethanesulfonyloxybenzoic acid methyl ester

: 1207343-88-1
3-chloro-4-dimethoxymethyl-2-(1-oxothianylideneamino)benzoic acid methyl ester

Guidance literature:: With caesium carbonate; 4,5-bis(diphenylphosphino)-9,9-dimethylxanthene; tris-(dibenzylideneacetone)dipalladium⁽⁰⁾; In toluene; for 3h; Reflux; Inert atmosphere;

Reference yield:

: 56962-10-8
2-chloro-3-hydroxybenzaldehyde

: 1207343-88-1
3-chloro-4-dimethoxymethyl-2-(1-oxothianylideneamino)benzoic acid methyl ester

Guidance literature:: Multi-step reaction with 6 steps

1: hydrogenchloride / methanol

2: bromine / chloroform / 20 °C / Cooling with ice

3: hydrogenchloride / methanol / Reflux

4: sodium acetate / palladium diacetate; (diphenylphosphin)ferrocene / 4 h / 90 - 100 °C / 6375.64 Torr / Autoclave

5: triethylamine / dichloromethane / 20 °C / Cooling with ice

6: caesium carbonate; 4,5-bis(diphenylphosphino)-9,9-dimethylxanthene / tris-(dibenzylideneacetone)dipalladium⁽⁰⁾ / toluene / 3 h / Reflux; Inert atmosphere

With bromine; sodium acetate; caesium carbonate; triethylamine; 4,5-bis(diphenylphosphino)-9,9-dimethylxanthene; hydrogenchloride; (diphenylphosphin)ferrocene; tris-(dibenzylideneacetone)dipalladium⁽⁰⁾; palladium diacetate; In methanol; dichloromethane; chloroform; toluene;

Reference yield:

: 860243-44-3
4-bromo-2-chloro-3-hydroxy-benzaldehyde

: 1207343-88-1
3-chloro-4-dimethoxymethyl-2-(1-oxothianylideneamino)benzoic acid methyl ester

Guidance literature:: Multi-step reaction with 4 steps

1: hydrogenchloride / methanol / Reflux

2: sodium acetate / palladium diacetate; (diphenylphosphin)ferrocene / 4 h / 90 - 100 °C / 6375.64 Torr / Autoclave

3: triethylamine / dichloromethane / 20 °C / Cooling with ice

4: caesium carbonate; 4,5-bis(diphenylphos4,5-bis(diphenylphosphino)-9,9-dimethylxanthenephino)-9,9-dimethylxanthene / tris-(dibenzylideneacetone)dipalladium⁽⁰⁾ / toluene / 3 h / Reflux; Inert atmosphere

With sodium acetate; caesium carbonate; triethylamine; 4,5-bis(diphenylphos4,5-bis(diphenylphosphino)-9,9-dimethylxanthenephino)-9,9-dimethylxanthene; hydrogenchloride; (diphenylphosphin)ferrocene; tris-(dibenzylideneacetone)dipalladium⁽⁰⁾; palladium diacetate; In methanol; dichloromethane; toluene;