C₃₀H₂₇NO₇S

Base Information

Chemical Name:C₃₀H₂₇NO₇S
CAS No.:144127-36-6
Molecular Formula:C₃₀H₂₇NO₇S
Molecular Weight:545.613
Hs Code.:

C<sub>30</sub>H<sub>27</sub>NO<sub>7</sub>S

Synonyms:C₃₀H₂₇NO₇S

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Chemical Property of C₃₀H₂₇NO₇S

Chemical Property:

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Technology Process of C₃₀H₂₇NO₇S

There total 8 articles about C₃₀H₂₇NO₇S 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:

: 699-12-7
2-(phenylthio)ethanol

: 144127-36-6
C₃₀H₂₇NO₇S

Guidance literature:: Multi-step reaction with 4 steps

1: cesium carbonate, 18-crown-6 / acetonitrile / 40 h / 25 °C

2: acetonitrile; benzene / 40 h / 25 °C

3: 100 percent / tetra-n-butylammonium fluoride (TBAF) / tetrahydrofuran / 0.33 h / 20 °C

4: 99 percent / m-CPBA / CH₂Cl₂ / 1 h / 25 °C

With 18-crown-6 ether; tetrabutyl ammonium fluoride; caesium carbonate; 3-chloro-benzenecarboperoxoic acid; In tetrahydrofuran; dichloromethane; acetonitrile; benzene;
DOI:10.1021/ja00049a022

Reference yield:

: 144154-92-7
C₂₆H₁₉NO₅

: 144127-36-6
C₃₀H₂₇NO₇S

Guidance literature:: Multi-step reaction with 7 steps

1: 90 percent / triethylamine / CH₂Cl₂ / 0.5 h / 20 °C

2: 100 percent / DMAP / CH₂Cl₂ / 48 h / 25 °C

3: 95 percent / n-Bu₃SnH, AIBN / benzene / 1 h / 70 °C

4: cesium carbonate, 18-crown-6 / acetonitrile / 40 h / 25 °C

5: acetonitrile; benzene / 40 h / 25 °C

6: 100 percent / tetra-n-butylammonium fluoride (TBAF) / tetrahydrofuran / 0.33 h / 20 °C

7: 99 percent / m-CPBA / CH₂Cl₂ / 1 h / 25 °C

With dmap; 18-crown-6 ether; 2,2'-azobis(isobutyronitrile); tetrabutyl ammonium fluoride; tri-n-butyl-tin hydride; caesium carbonate; triethylamine; 3-chloro-benzenecarboperoxoic acid; In tetrahydrofuran; dichloromethane; acetonitrile; benzene;
DOI:10.1021/ja00049a022

Reference yield:

: C₂₈H₂₃NO₄S

: 144127-36-6
C₃₀H₂₇NO₇S

Guidance literature:: Multi-step reaction with 3 steps

1: acetonitrile; benzene / 40 h / 25 °C

2: 100 percent / tetra-n-butylammonium fluoride (TBAF) / tetrahydrofuran / 0.33 h / 20 °C

3: 99 percent / m-CPBA / CH₂Cl₂ / 1 h / 25 °C

With tetrabutyl ammonium fluoride; 3-chloro-benzenecarboperoxoic acid; In tetrahydrofuran; dichloromethane; acetonitrile; benzene;
DOI:10.1021/ja00049a022