methyl (S)-4-<oxy>-α-<<(2,4,6-trimethylphenyl)sulfonyl>amino>benzeneacetate

Base Information

Chemical Name:methyl (S)-4-<oxy>-α-<<(2,4,6-trimethylphenyl)sulfonyl>amino>benzeneacetate
CAS No.:148838-41-9
Molecular Formula:C₂₆H₃₉NO₅SSi
Molecular Weight:505.751
Hs Code.:

methyl (S)-4-<<dimethyl(1,1,2-trimethylpropyl)silyl>oxy>-α-<<(2,4,6-trimethylphenyl)sulfonyl>amino>benzeneacetate

Synonyms:methyl (S)-4-<oxy>-α-<<(2,4,6-trimethylphenyl)sulfonyl>amino>benzeneacetate

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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 methyl (S)-4-<oxy>-α-<<(2,4,6-trimethylphenyl)sulfonyl>amino>benzeneacetate

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Technology Process of methyl (S)-4-<oxy>-α-<<(2,4,6-trimethylphenyl)sulfonyl>amino>benzeneacetate

There total 2 articles about methyl (S)-4-<oxy>-α-<<(2,4,6-trimethylphenyl)sulfonyl>amino>benzeneacetate 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: 68.0%

: 67-56-1
methanol

: 148838-35-1
(1S,2E,4S)-N-<2-bromo-1-<4-phenyl>-4-<(2-methoxyethoxy)methoxy>-2-pentenyl>-2,4,6-trimethylbenzenesulfonamide

: 87681-26-3
(2S)-2-<((Methoxyethoxy)methyl)oxy>propanoic Acid Methyl Ester

: 148838-41-9
methyl (S)-4-<oxy>-α-<<(2,4,6-trimethylphenyl)sulfonyl>amino>benzeneacetate

Guidance literature:: With oxygen; ozone; In dichloromethane; at -78 - -40 ℃;
DOI:10.1002/jlac.199719970121

Reference yield:

: N-[1-{4-[Dimethyl-(1,1,2-trimethyl-propyl)-silanyloxy]-phenyl}-meth-(E)-ylidene]-2,4,6-trimethyl-benzenesulfonamide

: 148838-41-9
methyl (S)-4-<oxy>-α-<<(2,4,6-trimethylphenyl)sulfonyl>amino>benzeneacetate

Guidance literature:: Multi-step reaction with 2 steps

1: 54 percent / tetrahydrofuran / -110 °C

2: O₃ / methanol; CH₂Cl₂

With ozone; In tetrahydrofuran; methanol; dichloromethane;