(S)-tert-butyl 5-chloro-2-(2-(4-methylphenylsulfonamido)ethyl)-1-oxo-2,3-dihydro-1H-indene-2-carboxylate

Base Information

Chemical Name:(S)-tert-butyl 5-chloro-2-(2-(4-methylphenylsulfonamido)ethyl)-1-oxo-2,3-dihydro-1H-indene-2-carboxylate
CAS No.:1078713-93-5
Molecular Formula:C₂₃H₂₆ClNO₅S
Molecular Weight:463.982
Hs Code.:

Synonyms:(S)-tert-butyl 5-chloro-2-(2-(4-methylphenylsulfonamido)ethyl)-1-oxo-2,3-dihydro-1H-indene-2-carboxylate

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Chemical Property of (S)-tert-butyl 5-chloro-2-(2-(4-methylphenylsulfonamido)ethyl)-1-oxo-2,3-dihydro-1H-indene-2-carboxylate

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Technology Process of (S)-tert-butyl 5-chloro-2-(2-(4-methylphenylsulfonamido)ethyl)-1-oxo-2,3-dihydro-1H-indene-2-carboxylate

There total 2 articles about (S)-tert-butyl 5-chloro-2-(2-(4-methylphenylsulfonamido)ethyl)-1-oxo-2,3-dihydro-1H-indene-2-carboxylate 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: 83.0%

: 871682-78-9
tert-butyl 5-chloro-1-oxo-2,3-dihydro-1H-indene-2-carboxylate

: 3634-89-7
N-(p-toluenesulfonyl)aziridine

: 1078713-93-5
(S)-tert-butyl 5-chloro-2-(2-(4-methylphenylsulfonamido)ethyl)-1-oxo-2,3-dihydro-1H-indene-2-carboxylate

Guidance literature:: With dipotassium hydrogenphosphate; C₄₅H₄₉N₂O₂⁽¹⁺⁾*Cl^(1-); In chloroform; o-xylene; water; at 2 ℃; for 12h; optical yield given as %ee; enantioselective reaction;
DOI:10.1039/b812369a

Reference yield:

: 871682-78-9
tert-butyl 5-chloro-1-oxo-2,3-dihydro-1H-indene-2-carboxylate

: 1078713-93-5
(S)-tert-butyl 5-chloro-2-(2-(4-methylphenylsulfonamido)ethyl)-1-oxo-2,3-dihydro-1H-indene-2-carboxylate

: C₂₃H₂₆ClNO₅S

Guidance literature:: With C₄₅H₄₉N₂O₂⁽¹⁺⁾*Cl^(1-); potassium carbonate; In chloroform; o-xylene; water; at 2 ℃; optical yield given as %ee; enantioselective reaction;
DOI:10.1039/b812369a