1-(thiophen-2-yl)-2-phenyl-4H-5,6,7,8-tetrahydrobenzo[b]thieno[3,2-c]pyran-4-one

Base Information

Chemical Name:1-(thiophen-2-yl)-2-phenyl-4H-5,6,7,8-tetrahydrobenzo[b]thieno[3,2-c]pyran-4-one
CAS No.:1384579-88-7
Molecular Formula:C₂₁H₁₆O₂S₂
Molecular Weight:364.489
Hs Code.:

Synonyms:1-(thiophen-2-yl)-2-phenyl-4H-5,6,7,8-tetrahydrobenzo[b]thieno[3,2-c]pyran-4-one

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Chemical Property of 1-(thiophen-2-yl)-2-phenyl-4H-5,6,7,8-tetrahydrobenzo[b]thieno[3,2-c]pyran-4-one

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Technology Process of 1-(thiophen-2-yl)-2-phenyl-4H-5,6,7,8-tetrahydrobenzo[b]thieno[3,2-c]pyran-4-one

There total 5 articles about 1-(thiophen-2-yl)-2-phenyl-4H-5,6,7,8-tetrahydrobenzo[b]thieno[3,2-c]pyran-4-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: 63.0%

: 6165-68-0
thiophene boronic acid

: 1384579-54-7
1-iodo-2-phenyl-4H-5,6,7,8-tetrahydrobenzo[b]thieno[3,2-c]pyran-4-one

: 1384579-88-7
1-(thiophen-2-yl)-2-phenyl-4H-5,6,7,8-tetrahydrobenzo[b]thieno[3,2-c]pyran-4-one

Guidance literature:: With palladium diacetate; potassium carbonate; In N,N-dimethyl-formamide; at 80 ℃; for 3.16667h; Inert atmosphere;
DOI:10.1016/j.bmcl.2012.04.109

Reference yield:

: 1309873-11-7
ethyl 2-iodo-4,5,6,7-tetrahydrobenzo[b]thiophene-3-carboxylate

: 1384579-88-7
1-(thiophen-2-yl)-2-phenyl-4H-5,6,7,8-tetrahydrobenzo[b]thieno[3,2-c]pyran-4-one

Guidance literature:: Multi-step reaction with 3 steps

1: copper(l) iodide; palladium 10% on activated carbon; triethylamine; triphenylphosphine / ethanol / 2.25 h / 60 °C / Inert atmosphere

2: iodine / dichloromethane / 0.08 h / 20 °C / Inert atmosphere

3: palladium diacetate; potassium carbonate / N,N-dimethyl-formamide / 3.17 h / 80 °C / Inert atmosphere

With copper(l) iodide; palladium 10% on activated carbon; iodine; palladium diacetate; potassium carbonate; triethylamine; triphenylphosphine; In ethanol; dichloromethane; N,N-dimethyl-formamide; 3: Suzuki reaction;
DOI:10.1016/j.bmcl.2012.04.109

Reference yield:

: 1384579-39-8
ethyl 2-(phenylethynyl)-4,5,6,7-tetrahydrobenzo[b]thiophene-3-carboxylate

: 1384579-88-7
1-(thiophen-2-yl)-2-phenyl-4H-5,6,7,8-tetrahydrobenzo[b]thieno[3,2-c]pyran-4-one

Guidance literature:: Multi-step reaction with 2 steps

1: iodine / dichloromethane / 0.08 h / 20 °C / Inert atmosphere

2: palladium diacetate; potassium carbonate / N,N-dimethyl-formamide / 3.17 h / 80 °C / Inert atmosphere

With iodine; palladium diacetate; potassium carbonate; In dichloromethane; N,N-dimethyl-formamide; 2: Suzuki reaction;
DOI:10.1016/j.bmcl.2012.04.109