methyl 4-(2-fluorophenyl)-2-(2,4,6-triisopropylphenylsulfonylimino)but-3-enoate

Base Information

Chemical Name:methyl 4-(2-fluorophenyl)-2-(2,4,6-triisopropylphenylsulfonylimino)but-3-enoate
CAS No.:1239317-27-1
Molecular Formula:C₂₆H₃₂FNO₄S
Molecular Weight:473.609
Hs Code.:

Synonyms:methyl 4-(2-fluorophenyl)-2-(2,4,6-triisopropylphenylsulfonylimino)but-3-enoate

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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 4-(2-fluorophenyl)-2-(2,4,6-triisopropylphenylsulfonylimino)but-3-enoate

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Technology Process of methyl 4-(2-fluorophenyl)-2-(2,4,6-triisopropylphenylsulfonylimino)but-3-enoate

There total 1 articles about methyl 4-(2-fluorophenyl)-2-(2,4,6-triisopropylphenylsulfonylimino)but-3-enoate 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: 49.0%

: 1239317-44-2
(E)-methyl 4-(2-fluorophenyl)-2-oxobut-3-enoate

: 105536-22-9
2,4,6-triisopropylbenzene sulfonamide

: 1239317-27-1
methyl 4-(2-fluorophenyl)-2-(2,4,6-triisopropylphenylsulfonylimino)but-3-enoate

Guidance literature:: With titanium tetrachloride; triethylamine; In dichloromethane; at 0 - 20 ℃;
DOI:10.1002/anie.201000755

Reference yield:

: 1239317-27-1
methyl 4-(2-fluorophenyl)-2-(2,4,6-triisopropylphenylsulfonylimino)but-3-enoate

: C₃₀H₂₂OS

: (4R,5S)-methyl 5-benzoyl-4-(2-fluorophenyl)-1-(2,4,6-triisopropylphenylsulfonyl)-4,5-dihydro-1H-pyrrole-2-carboxylate

: 1239317-36-2
(4S,5R)-methyl 5-benzoyl-4-(2-fluorophenyl)-1-(2,4,6-triisopropylphenylsulfonyl)-4,5-dihydro-1H-pyrrole-2-carboxylate

Guidance literature:: In dichloromethane; toluene; at -80 - 20 ℃; optical yield given as %ee; enantioselective reaction;
DOI:10.1002/anie.201000755