methyl 2-({2-[4-(benzyloxy)phenyl]ethyl}thio)-3-[4-(2-{4-[(methylsulfonyl)oxy]-phenoxy}ethyl)phenyl]propanoate

Base Information

Chemical Name:methyl 2-({2-[4-(benzyloxy)phenyl]ethyl}thio)-3-[4-(2-{4-[(methylsulfonyl)oxy]-phenoxy}ethyl)phenyl]propanoate
CAS No.:549494-37-3
Molecular Formula:C₃₄H₃₆O₇S₂
Molecular Weight:620.788
Hs Code.:

Synonyms:methyl 2-({2-[4-(benzyloxy)phenyl]ethyl}thio)-3-[4-(2-{4-[(methylsulfonyl)oxy]-phenoxy}ethyl)phenyl]propanoate

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Chemical Property of methyl 2-({2-[4-(benzyloxy)phenyl]ethyl}thio)-3-[4-(2-{4-[(methylsulfonyl)oxy]-phenoxy}ethyl)phenyl]propanoate

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Technology Process of methyl 2-({2-[4-(benzyloxy)phenyl]ethyl}thio)-3-[4-(2-{4-[(methylsulfonyl)oxy]-phenoxy}ethyl)phenyl]propanoate

There total 5 articles about methyl 2-({2-[4-(benzyloxy)phenyl]ethyl}thio)-3-[4-(2-{4-[(methylsulfonyl)oxy]-phenoxy}ethyl)phenyl]propanoate 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:

: 104-10-9
2-(4'-aminophenyl)ethyl alcohol

: 549494-37-3
methyl 2-({2-[4-(benzyloxy)phenyl]ethyl}thio)-3-[4-(2-{4-[(methylsulfonyl)oxy]-phenoxy}ethyl)phenyl]propanoate

Guidance literature:: Multi-step reaction with 5 steps

1.1: hydrogenchloride; sodium nitrite / water; acetone / 1 h / 0 °C

1.2: 0 - 20 °C

2.1: di-isopropyl azodicarboxylate; triphenylphosphine / toluene

3.1: dimethylsulfide; boron trifluoride diethyl etherate / dichloromethane / 48 h / 20 °C

4.1: triethylamine / dichloromethane / 2 h / -20 - 20 °C

5.1: potassium carbonate / DMF (N,N-dimethyl-formamide) / 20 °C

With hydrogenchloride; dimethylsulfide; di-isopropyl azodicarboxylate; boron trifluoride diethyl etherate; potassium carbonate; triethylamine; triphenylphosphine; sodium nitrite; In DMF (N,N-dimethyl-formamide); dichloromethane; water; acetone; toluene;

Reference yield:

: 549494-35-1
methyl 2-chloro-3-(4-[2-(4-hydroxyphenoxy)ethyl]phenyl)propanoate

: 549494-37-3
methyl 2-({2-[4-(benzyloxy)phenyl]ethyl}thio)-3-[4-(2-{4-[(methylsulfonyl)oxy]-phenoxy}ethyl)phenyl]propanoate

Guidance literature:: Multi-step reaction with 2 steps

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

2: potassium carbonate / DMF (N,N-dimethyl-formamide) / 20 °C

With potassium carbonate; triethylamine; In DMF (N,N-dimethyl-formamide); dichloromethane;

Reference yield:

: 103-16-2
4-Benzyloxyphenol

: 549494-37-3
methyl 2-({2-[4-(benzyloxy)phenyl]ethyl}thio)-3-[4-(2-{4-[(methylsulfonyl)oxy]-phenoxy}ethyl)phenyl]propanoate

Guidance literature:: Multi-step reaction with 4 steps

1: di-isopropyl azodicarboxylate; triphenylphosphine / toluene

2: dimethylsulfide; boron trifluoride diethyl etherate / dichloromethane / 48 h / 20 °C

3: triethylamine / dichloromethane / 2 h / -20 - 20 °C

4: potassium carbonate / DMF (N,N-dimethyl-formamide) / 20 °C

With dimethylsulfide; di-isopropyl azodicarboxylate; boron trifluoride diethyl etherate; potassium carbonate; triethylamine; triphenylphosphine; In DMF (N,N-dimethyl-formamide); dichloromethane; toluene;