(S)-2,5,7,8-tetramethyl-2-(1-phenyl-1H-imidazole-2-carbonyl)chroman-6-yl-4-methylbenzenesulfonate

Base Information

Chemical Name:(S)-2,5,7,8-tetramethyl-2-(1-phenyl-1H-imidazole-2-carbonyl)chroman-6-yl-4-methylbenzenesulfonate
CAS No.:1581710-02-2
Molecular Formula:C₃₀H₃₀N₂O₅S
Molecular Weight:530.645
Hs Code.:

Synonyms:(S)-2,5,7,8-tetramethyl-2-(1-phenyl-1H-imidazole-2-carbonyl)chroman-6-yl-4-methylbenzenesulfonate

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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 (S)-2,5,7,8-tetramethyl-2-(1-phenyl-1H-imidazole-2-carbonyl)chroman-6-yl-4-methylbenzenesulfonate

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Technology Process of (S)-2,5,7,8-tetramethyl-2-(1-phenyl-1H-imidazole-2-carbonyl)chroman-6-yl-4-methylbenzenesulfonate

There total 2 articles about (S)-2,5,7,8-tetramethyl-2-(1-phenyl-1H-imidazole-2-carbonyl)chroman-6-yl-4-methylbenzenesulfonate 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: 99.0%

: 1581709-96-7
4-hydroxy-2,3,6-trimethyl-5-[3-methyl-4-oxo-4-(1-phenyl-1H-imidazol-2-yl)butyl]phenyl 4-methylbenzenesulfonate

: 1581710-02-2
(S)-2,5,7,8-tetramethyl-2-(1-phenyl-1H-imidazole-2-carbonyl)chroman-6-yl-4-methylbenzenesulfonate

Guidance literature:: With Cumene hydroperoxide; C₉₂H₄₄F₅₂N⁽¹⁺⁾*I^(1-); In diethyl ether; at 20 ℃; for 0.75h; enantioselective reaction;
DOI:10.1126/science.1254976

Reference yield:

: 1581709-96-7
4-hydroxy-2,3,6-trimethyl-5-[3-methyl-4-oxo-4-(1-phenyl-1H-imidazol-2-yl)butyl]phenyl 4-methylbenzenesulfonate

: 1581710-02-2
(S)-2,5,7,8-tetramethyl-2-(1-phenyl-1H-imidazole-2-carbonyl)chroman-6-yl-4-methylbenzenesulfonate

: 1581710-01-1
C₃₀H₃₀N₂O₅S

Guidance literature:: With tert.-butylhydroperoxide; C₁₀₀H₅₆F₂₄N⁽¹⁺⁾*I^(1-); In tert-butyl methyl ether; at 20 ℃; for 3h; Overall yield = 99 %; enantioselective reaction;
DOI:10.1126/science.1254976