methyl 4-<<4-acetyl-3-<<(4-methylphenyl)sulfonyl>oxy>-2-(3-acetylpropyl)phenoxy>methyl>-3-methoxybenzoate

Base Information

Chemical Name:methyl 4-<<4-acetyl-3-<<(4-methylphenyl)sulfonyl>oxy>-2-(3-acetylpropyl)phenoxy>methyl>-3-methoxybenzoate
CAS No.:118683-94-6
Molecular Formula:C₃₀H₃₂O₉S
Molecular Weight:568.645
Hs Code.:

Synonyms:methyl 4-<<4-acetyl-3-<<(4-methylphenyl)sulfonyl>oxy>-2-(3-acetylpropyl)phenoxy>methyl>-3-methoxybenzoate

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Chemical Property of methyl 4-<<4-acetyl-3-<<(4-methylphenyl)sulfonyl>oxy>-2-(3-acetylpropyl)phenoxy>methyl>-3-methoxybenzoate

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Technology Process of methyl 4-<<4-acetyl-3-<<(4-methylphenyl)sulfonyl>oxy>-2-(3-acetylpropyl)phenoxy>methyl>-3-methoxybenzoate

There total 5 articles about methyl 4-<<4-acetyl-3-<<(4-methylphenyl)sulfonyl>oxy>-2-(3-acetylpropyl)phenoxy>methyl>-3-methoxybenzoate 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:

: 38987-00-7
2,4-dihydroxy-3-allylacetophenone

: 118683-94-6
methyl 4-<<4-acetyl-3-<<(4-methylphenyl)sulfonyl>oxy>-2-(3-acetylpropyl)phenoxy>methyl>-3-methoxybenzoate

Guidance literature:: Multi-step reaction with 5 steps

1: 78 percent / K₂CO₃ / acetone / 48 h / Heating

2: 84 percent / K₂CO₃ / acetone / 12 h / Heating

3: 1) O₃, 2) Me₂S / 1) CH₂Cl₂, MeOH, -78 deg C, 30 min, 2) rt, 30 min

4: 65 percent / tetrahydrofuran / 16 h / Heating

5: 70 percent / H₂ / PtO₂ (prereduced) / ethyl acetate / 3 h / 760 Torr / Ambient temperature

With dimethylsulfide; hydrogen; potassium carbonate; ozone; platinum(IV) oxide; In tetrahydrofuran; ethyl acetate; acetone;
DOI:10.1021/jm00124a014

Reference yield:

: 70264-94-7
methyl 4-(bromomethyl)-3-methoxybenzoate

: 118683-94-6
methyl 4-<<4-acetyl-3-<<(4-methylphenyl)sulfonyl>oxy>-2-(3-acetylpropyl)phenoxy>methyl>-3-methoxybenzoate

Guidance literature:: Multi-step reaction with 5 steps

1: 78 percent / K₂CO₃ / acetone / 48 h / Heating

2: 84 percent / K₂CO₃ / acetone / 12 h / Heating

3: 1) O₃, 2) Me₂S / 1) CH₂Cl₂, MeOH, -78 deg C, 30 min, 2) rt, 30 min

4: 65 percent / tetrahydrofuran / 16 h / Heating

5: 70 percent / H₂ / PtO₂ (prereduced) / ethyl acetate / 3 h / 760 Torr / Ambient temperature

With dimethylsulfide; hydrogen; potassium carbonate; ozone; platinum(IV) oxide; In tetrahydrofuran; ethyl acetate; acetone;
DOI:10.1021/jm00124a014

Reference yield:

: 118683-90-2
methyl 4-<(4-acetyl-3-hydroxy-2-prop-2-enylphenoxy)methyl>-3-methoxybenzoate

: 118683-94-6
methyl 4-<<4-acetyl-3-<<(4-methylphenyl)sulfonyl>oxy>-2-(3-acetylpropyl)phenoxy>methyl>-3-methoxybenzoate

Guidance literature:: Multi-step reaction with 4 steps

1: 84 percent / K₂CO₃ / acetone / 12 h / Heating

2: 1) O₃, 2) Me₂S / 1) CH₂Cl₂, MeOH, -78 deg C, 30 min, 2) rt, 30 min

3: 65 percent / tetrahydrofuran / 16 h / Heating

4: 70 percent / H₂ / PtO₂ (prereduced) / ethyl acetate / 3 h / 760 Torr / Ambient temperature

With dimethylsulfide; hydrogen; potassium carbonate; ozone; platinum(IV) oxide; In tetrahydrofuran; ethyl acetate; acetone;
DOI:10.1021/jm00124a014