(+)-(R)-6-[(1S,2R)-1,2-bis-(tert-butyl-dimethylsilanyloxy)but-3-enyl]-1-(2-nitrobenzenesulfonyl)-1,2,3,6-tetrahydropyridine

Base Information

Chemical Name:(+)-(R)-6-[(1S,2R)-1,2-bis-(tert-butyl-dimethylsilanyloxy)but-3-enyl]-1-(2-nitrobenzenesulfonyl)-1,2,3,6-tetrahydropyridine
CAS No.:301805-14-1
Molecular Formula:C₂₇H₄₆N₂O₆SSi₂
Molecular Weight:582.909
Hs Code.:

Synonyms:(+)-(R)-6-[(1S,2R)-1,2-bis-(tert-butyl-dimethylsilanyloxy)but-3-enyl]-1-(2-nitrobenzenesulfonyl)-1,2,3,6-tetrahydropyridine

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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 (+)-(R)-6-[(1S,2R)-1,2-bis-(tert-butyl-dimethylsilanyloxy)but-3-enyl]-1-(2-nitrobenzenesulfonyl)-1,2,3,6-tetrahydropyridine

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Technology Process of (+)-(R)-6-[(1S,2R)-1,2-bis-(tert-butyl-dimethylsilanyloxy)but-3-enyl]-1-(2-nitrobenzenesulfonyl)-1,2,3,6-tetrahydropyridine

There total 9 articles about (+)-(R)-6-[(1S,2R)-1,2-bis-(tert-butyl-dimethylsilanyloxy)but-3-enyl]-1-(2-nitrobenzenesulfonyl)-1,2,3,6-tetrahydropyridine 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: 100.0%

: 301805-13-0
(-)-N-(but-3-enyl)-N-{(1R,4R,5S)-4,5-bis-(tert-butyldimethylsilanyloxy)cyclopent-2-enyl}-2-nitrobenzenesulfonamide

: 301805-14-1
(+)-(R)-6-[(1S,2R)-1,2-bis-(tert-butyl-dimethylsilanyloxy)but-3-enyl]-1-(2-nitrobenzenesulfonyl)-1,2,3,6-tetrahydropyridine

Guidance literature:: With Grubbs catalyst first generation; ethene; In dichloromethane;
DOI:10.1016/S0040-4020(02)00832-3

Reference yield:

: 90870-33-0
N-(2-nitrobenzenesulfonyl)-N-(but-3-enyl)amine

: 301805-14-1
(+)-(R)-6-[(1S,2R)-1,2-bis-(tert-butyl-dimethylsilanyloxy)but-3-enyl]-1-(2-nitrobenzenesulfonyl)-1,2,3,6-tetrahydropyridine

Guidance literature:: Multi-step reaction with 4 steps

1: 93 percent / Et₃N; [Pd₂(dba)3]*CHCl₃; (R,R)-N,N'-bis[2-(PPh₂)benzoyl]-1,2-diaminocyclohexane / tetrahydrofuran / -10 - 0 °C

2: acetic acid / H₂O / 80 - 100 °C

3: 85.2 mg / imidazole / dimethylformamide

4: 100 percent / ethylene; Cl₂(PCy₃)2Ru=CHPh / CH₂Cl₂

With 1H-imidazole; tris-(dibenzylideneacetone)dipalladium⁽⁰⁾; Grubbs catalyst first generation; ethene; acetic acid; (1R,2R)-1,2-bis[(2-diphenylphosphanyl)benzoylamino]cyclohexane; triethylamine; In tetrahydrofuran; dichloromethane; water; N,N-dimethyl-formamide;
DOI:10.1016/S0040-4020(02)00832-3

Reference yield:

: 501416-20-2
N-but-3-enyl-N-(4,5-dihydroxy-cyclopent-2-enyl)-2-nitro-benzenesulfonamide

: 301805-14-1
(+)-(R)-6-[(1S,2R)-1,2-bis-(tert-butyl-dimethylsilanyloxy)but-3-enyl]-1-(2-nitrobenzenesulfonyl)-1,2,3,6-tetrahydropyridine

Guidance literature:: Multi-step reaction with 2 steps

1: 85.2 mg / imidazole / dimethylformamide

2: 100 percent / ethylene; Cl₂(PCy₃)2Ru=CHPh / CH₂Cl₂

With 1H-imidazole; Grubbs catalyst first generation; ethene; In dichloromethane; N,N-dimethyl-formamide;
DOI:10.1016/S0040-4020(02)00832-3