C₃₃H₃₅N₂O₇⁽¹⁺⁾*Cl^(1-)

Base Information

Chemical Name:C₃₃H₃₅N₂O₇⁽¹⁺⁾*Cl^(1-)
CAS No.:1079889-34-1
Molecular Formula:C₃₃H₃₅N₂O₇*Cl
Molecular Weight:607.103
Hs Code.:

C<sub>33</sub>H<sub>35</sub>N<sub>2</sub>O<sub>7</sub><sup>(1+)</sup>*Cl<sup>(1-)</sup>

Synonyms:C₃₃H₃₅N₂O₇⁽¹⁺⁾*Cl^(1-)

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Chemical Property of C₃₃H₃₅N₂O₇⁽¹⁺⁾*Cl^(1-)

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Technology Process of C₃₃H₃₅N₂O₇⁽¹⁺⁾*Cl^(1-)

There total 7 articles about C₃₃H₃₅N₂O₇⁽¹⁺⁾*Cl^(1-) 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:

: C₄₁H₅₁N₂O₇⁽¹⁺⁾*Cl^(1-)

: 1079889-34-1
C₃₃H₃₅N₂O₇⁽¹⁺⁾*Cl^(1-)

Guidance literature:: C₄₁H₅₁N₂O₇⁽¹⁺⁾*Cl^(1-); With trifluoroacetic acid; In dichloromethane; at 25 ℃; for 1h;

In methanol; dichloromethane; at 20 ℃;
DOI:10.1021/jo800902j

Reference yield:

: 1214-24-0
3,6-dihydroxy-xanthen-9-one

: 1079889-34-1
C₃₃H₃₅N₂O₇⁽¹⁺⁾*Cl^(1-)

Guidance literature:: Multi-step reaction with 6 steps

1.1: pyridine / dichloromethane / 0.25 h / 0 °C

1.2: 24 h / 0 - 20 °C

2.1: dimethyl sulfoxide / 12 h / 90 °C

3.1: tetrahydrofuran / 12 h / 0 - 20 °C

3.2: 0.17 h

4.1: boron tribromide / dichloromethane / -78 - 20 °C

4.2: Amberlite IRA-400 (CI) ion exchange resin / 1 h / 20 °C

5.1: caesium carbonate; tetra-(n-butyl)ammonium iodide / N,N-dimethyl-formamide / 12 h / 25 °C

6.1: trifluoroacetic acid / dichloromethane / 1 h / 25 °C

With pyridine; boron tribromide; tetra-(n-butyl)ammonium iodide; caesium carbonate; trifluoroacetic acid; In tetrahydrofuran; dichloromethane; dimethyl sulfoxide; N,N-dimethyl-formamide;

Reference yield:

: 131-55-5
2,2',4,4'-tetrahydroxybenzophenone

: 1079889-34-1
C₃₃H₃₅N₂O₇⁽¹⁺⁾*Cl^(1-)

Guidance literature:: Multi-step reaction with 7 steps

1.1: water / 6 h / 200 °C / Autoclave

2.1: pyridine / dichloromethane / 0.25 h / 0 °C

2.2: 24 h / 0 - 20 °C

3.1: dimethyl sulfoxide / 12 h / 90 °C

4.1: tetrahydrofuran / 12 h / 0 - 20 °C

4.2: 0.17 h

5.1: boron tribromide / dichloromethane / -78 - 20 °C

5.2: Amberlite IRA-400 (CI) ion exchange resin / 1 h / 20 °C

6.1: caesium carbonate; tetra-(n-butyl)ammonium iodide / N,N-dimethyl-formamide / 12 h / 25 °C

7.1: trifluoroacetic acid / dichloromethane / 1 h / 25 °C

With pyridine; boron tribromide; tetra-(n-butyl)ammonium iodide; caesium carbonate; trifluoroacetic acid; In tetrahydrofuran; dichloromethane; water; dimethyl sulfoxide; N,N-dimethyl-formamide;