2′,3′-diphenyl-2H-spiro[benzo[d]isothiazole-3,1′-cyclopenta[b]naphthalene]1,1-dioxide

Base Information

Chemical Name:2′,3′-diphenyl-2H-spiro[benzo[d]isothiazole-3,1′-cyclopenta[b]naphthalene]1,1-dioxide
CAS No.:1568952-44-2
Molecular Formula:C₃₁H₂₁NO₂S
Molecular Weight:471.579
Hs Code.:

Synonyms:2′,3′-diphenyl-2H-spiro[benzo[d]isothiazole-3,1′-cyclopenta[b]naphthalene]1,1-dioxide

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Chemical Property of 2′,3′-diphenyl-2H-spiro[benzo[d]isothiazole-3,1′-cyclopenta[b]naphthalene]1,1-dioxide

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Technology Process of 2′,3′-diphenyl-2H-spiro[benzo[d]isothiazole-3,1′-cyclopenta[b]naphthalene]1,1-dioxide

There total 3 articles about 2′,3′-diphenyl-2H-spiro[benzo[d]isothiazole-3,1′-cyclopenta[b]naphthalene]1,1-dioxide 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: 99.0%

: 1421371-61-0
3-(naphthalen-2-yl)benzo[d]isothiazole 1,1-dioxide

: 501-65-5
diphenyl acetylene

: 1568952-44-2
2′,3′-diphenyl-2H-spiro[benzo[d]isothiazole-3,1′-cyclopenta[b]naphthalene]1,1-dioxide

Guidance literature:: With dichloro(pentamethylcyclopentadienyl)rhodium (III) dimer; F₆Sb⁽¹⁺⁾*Ag⁽¹⁺⁾; In 1,2-dichloro-ethane; at 80 ℃; for 15h; regioselective reaction; Inert atmosphere;
DOI:10.1002/chem.201303372

Reference yield:

: 81-07-2
saccharin

: 1568952-44-2
2′,3′-diphenyl-2H-spiro[benzo[d]isothiazole-3,1′-cyclopenta[b]naphthalene]1,1-dioxide

Guidance literature:: Multi-step reaction with 2 steps

1: tetrahydrofuran / 4 h / -78 °C / Inert atmosphere

2: dichloro(pentamethylcyclopentadienyl)rhodium (III) dimer; silver hexafluoroantimonate / chlorobenzene / 3 h / 80 °C / Inert atmosphere; Sealed tube; Glovebox; Darkness

With silver hexafluoroantimonate; dichloro(pentamethylcyclopentadienyl)rhodium (III) dimer; In tetrahydrofuran; chlorobenzene;
DOI:10.1002/chem.201504998

Reference yield:

: 4541-70-2
2-naphthyllithium

: 1568952-44-2
2′,3′-diphenyl-2H-spiro[benzo[d]isothiazole-3,1′-cyclopenta[b]naphthalene]1,1-dioxide

Guidance literature:: Multi-step reaction with 2 steps

1: tetrahydrofuran / 4 h / -78 °C / Inert atmosphere

2: dichloro(pentamethylcyclopentadienyl)rhodium (III) dimer; silver hexafluoroantimonate / chlorobenzene / 3 h / 80 °C / Inert atmosphere; Sealed tube; Glovebox; Darkness

With silver hexafluoroantimonate; dichloro(pentamethylcyclopentadienyl)rhodium (III) dimer; In tetrahydrofuran; chlorobenzene;
DOI:10.1002/chem.201504998