(R)-6-[(S)-2-(tert-butyl-dimethyl-silanyloxy)-but-3-enyl]-1-(2-nitro-benzenesulfonyl)-1,2,3,6-tetrahydro-pyridine

Base Information

Chemical Name:(R)-6-[(S)-2-(tert-butyl-dimethyl-silanyloxy)-but-3-enyl]-1-(2-nitro-benzenesulfonyl)-1,2,3,6-tetrahydro-pyridine
CAS No.:317809-50-0
Molecular Formula:C₂₁H₃₂N₂O₅SSi
Molecular Weight:452.647
Hs Code.:

Synonyms:(R)-6-[(S)-2-(tert-butyl-dimethyl-silanyloxy)-but-3-enyl]-1-(2-nitro-benzenesulfonyl)-1,2,3,6-tetrahydro-pyridine

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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-[(S)-2-(tert-butyl-dimethyl-silanyloxy)-but-3-enyl]-1-(2-nitro-benzenesulfonyl)-1,2,3,6-tetrahydro-pyridine

Chemical Property:

Purity/Quality:: 98% ^*data from raw suppliers

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Technology Process of (R)-6-[(S)-2-(tert-butyl-dimethyl-silanyloxy)-but-3-enyl]-1-(2-nitro-benzenesulfonyl)-1,2,3,6-tetrahydro-pyridine

There total 4 articles about (R)-6-[(S)-2-(tert-butyl-dimethyl-silanyloxy)-but-3-enyl]-1-(2-nitro-benzenesulfonyl)-1,2,3,6-tetrahydro-pyridine 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: 95.0%

: 317809-49-7
N-but-3-enyl-N-[(1R,4S)-4-(tert-butyl-dimethyl-silanyloxy)-cyclopent-2-enyl]-2-nitro-benzenesulfonamide

: 317809-50-0
(R)-6-[(S)-2-(tert-butyl-dimethyl-silanyloxy)-but-3-enyl]-1-(2-nitro-benzenesulfonyl)-1,2,3,6-tetrahydro-pyridine

Guidance literature:: With ethene; Grubbs catalyst first generation; In dichloromethane; at 20 ℃; for 24h;
DOI:10.1021/ol000188r

Reference yield:

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

: 317809-50-0
(R)-6-[(S)-2-(tert-butyl-dimethyl-silanyloxy)-but-3-enyl]-1-(2-nitro-benzenesulfonyl)-1,2,3,6-tetrahydro-pyridine

Guidance literature:: Multi-step reaction with 3 steps

1.1: NaH / dimethylformamide; various solvent(s) / 0.5 h / 0 - 20 °C

1.2: 83 percent / PPh₃ / Pd(OAc)2 / dimethylformamide; various solvent(s) / 15 h

2.1: 98 percent / imidazole / dimethylformamide / 15 h / 20 °C

3.1: 95 percent / CH₂=CH₂ / PhCH=RuCl₂(PCy₃)2 / CH₂Cl₂ / 24 h / 20 °C

With 1H-imidazole; ethene; sodium hydride; Grubbs catalyst first generation; In dichloromethane; N,N-dimethyl-formamide; 1.1: deprotonation / 1.2: Alkylation / 2.1: silylation / 3.1: Rearrangement;
DOI:10.1021/ol000188r

Reference yield:

: 60410-16-4
(1R,4S)-4-hydroxy-2-cyclopentene-1-yl acetate

: 317809-50-0
(R)-6-[(S)-2-(tert-butyl-dimethyl-silanyloxy)-but-3-enyl]-1-(2-nitro-benzenesulfonyl)-1,2,3,6-tetrahydro-pyridine

Guidance literature:: Multi-step reaction with 3 steps

1.1: NaH / dimethylformamide; various solvent(s) / 0.5 h / 0 - 20 °C

1.2: 83 percent / PPh₃ / Pd(OAc)2 / dimethylformamide; various solvent(s) / 15 h

2.1: 98 percent / imidazole / dimethylformamide / 15 h / 20 °C

3.1: 95 percent / CH₂=CH₂ / PhCH=RuCl₂(PCy₃)2 / CH₂Cl₂ / 24 h / 20 °C

With 1H-imidazole; ethene; sodium hydride; Grubbs catalyst first generation; In dichloromethane; N,N-dimethyl-formamide; 1.1: deprotonation / 1.2: Alkylation / 2.1: silylation / 3.1: Rearrangement;
DOI:10.1021/ol000188r