6-oxo-7,8,9,10,11,12-hexahydro-6H-cycloocta[c]chromen-3-yl 4-fluorobenzenesulfonate

Base Information

Chemical Name:6-oxo-7,8,9,10,11,12-hexahydro-6H-cycloocta[c]chromen-3-yl 4-fluorobenzenesulfonate
CAS No.:1621574-92-2
Molecular Formula:C₂₁H₁₉FO₅S
Molecular Weight:402.443
Hs Code.:

Synonyms:6-oxo-7,8,9,10,11,12-hexahydro-6H-cycloocta[c]chromen-3-yl 4-fluorobenzenesulfonate

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Business phase:: The product has achieved commercial mass production^*data from LookChem market partment

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Chemical Property of 6-oxo-7,8,9,10,11,12-hexahydro-6H-cycloocta[c]chromen-3-yl 4-fluorobenzenesulfonate

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Technology Process of 6-oxo-7,8,9,10,11,12-hexahydro-6H-cycloocta[c]chromen-3-yl 4-fluorobenzenesulfonate

There total 3 articles about 6-oxo-7,8,9,10,11,12-hexahydro-6H-cycloocta[c]chromen-3-yl 4-fluorobenzenesulfonate 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: 89.0%

: 319929-12-9
C₁₅H₁₆O₃

: 349-88-2
4-Fluorobenzenesulfonyl chloride

: 1621574-92-2
6-oxo-7,8,9,10,11,12-hexahydro-6H-cycloocta[c]chromen-3-yl 4-fluorobenzenesulfonate

Guidance literature:: With triethylamine; In dichloromethane; at 0 - 20 ℃; for 1h;
DOI:10.1002/ardp.201600243

Reference yield:

: 502-49-8
cycloactanone

: 1621574-92-2
6-oxo-7,8,9,10,11,12-hexahydro-6H-cycloocta[c]chromen-3-yl 4-fluorobenzenesulfonate

Guidance literature:: Multi-step reaction with 3 steps

1: sodium hydride / mineral oil; benzene / Reflux

2: trifluoroacetic acid; sulfuric acid / 3.5 h / 0 - 20 °C

3: triethylamine / dichloromethane / 1 h / 0 - 20 °C

With sulfuric acid; sodium hydride; triethylamine; trifluoroacetic acid; In dichloromethane; mineral oil; benzene;
DOI:10.1016/j.ejmech.2014.06.064

Reference yield:

: 4017-56-5
ethyl 2-oxocyclooctane-1-carboxylate

: 1621574-92-2
6-oxo-7,8,9,10,11,12-hexahydro-6H-cycloocta[c]chromen-3-yl 4-fluorobenzenesulfonate

Guidance literature:: Multi-step reaction with 2 steps

1: trifluoroacetic acid; sulfuric acid / 3 h / 0 - 20 °C

2: triethylamine / dichloromethane / 1 h / 0 - 20 °C

With sulfuric acid; triethylamine; trifluoroacetic acid; In dichloromethane;
DOI:10.1002/ardp.201600243