C₂₀H₁₈O₄S

Base Information

Chemical Name:C₂₀H₁₈O₄S
CAS No.:1400883-61-5
Molecular Formula:C₂₀H₁₈O₄S
Molecular Weight:354.427
Hs Code.:

C<sub>20</sub>H<sub>18</sub>O<sub>4</sub>S

Synonyms:C₂₀H₁₈O₄S

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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 C₂₀H₁₈O₄S

Chemical Property:

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Technology Process of C₂₀H₁₈O₄S

There total 5 articles about C₂₀H₁₈O₄S 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: 67.0%

: 26321-31-3
2-(p-tolyloxy)phenol

: 98-59-9
p-toluenesulfonyl chloride

: 1400883-61-5
C₂₀H₁₈O₄S

Guidance literature:: With pyridine; at 45 ℃; for 12h; Sealed tube;
DOI:10.1021/ol302166n

Reference yield:

: 446-52-6
2-Fluorobenzaldehyde

: 1400883-61-5
C₂₀H₁₈O₄S

Guidance literature:: Multi-step reaction with 4 steps

1: potassium carbonate / N,N-dimethyl acetamide / 2 h / 160 °C / Sealed tube

2: 3-chloro-benzenecarboperoxoic acid / dichloromethane / 2 h / 20 °C

3: hydrogenchloride / methanol / 1 h / 20 °C

4: pyridine / 12 h / 45 °C / Sealed tube

With pyridine; hydrogenchloride; potassium carbonate; 3-chloro-benzenecarboperoxoic acid; In methanol; dichloromethane; N,N-dimethyl acetamide;
DOI:10.1021/ol302166n

Reference yield:

: 67698-66-2
2-(2-methylphenoxy)benzaldehyde

: 1400883-61-5
C₂₀H₁₈O₄S

Guidance literature:: Multi-step reaction with 3 steps

1: 3-chloro-benzenecarboperoxoic acid / dichloromethane / 2 h / 20 °C

2: hydrogenchloride / methanol / 1 h / 20 °C

3: pyridine / 12 h / 45 °C / Sealed tube

With pyridine; hydrogenchloride; 3-chloro-benzenecarboperoxoic acid; In methanol; dichloromethane;
DOI:10.1021/ol302166n