N-but-3-enyl-N-[6-(tert-butyl-dimethyl-silanyloxy)-4-hydroxy-cyclohept-2-enyl]-2-nitro-benzenesulfonamide

Base Information

Chemical Name:N-but-3-enyl-N-[6-(tert-butyl-dimethyl-silanyloxy)-4-hydroxy-cyclohept-2-enyl]-2-nitro-benzenesulfonamide
CAS No.:482376-67-0
Molecular Formula:C₂₃H₃₆N₂O₆SSi
Molecular Weight:496.7
Hs Code.:

<i>N</i>-but-3-enyl-<i>N</i>-[6-(<i>tert</i>-butyl-dimethyl-silanyloxy)-4-hydroxy-cyclohept-2-enyl]-2-nitro-benzenesulfonamide

Synonyms:N-but-3-enyl-N-[6-(tert-butyl-dimethyl-silanyloxy)-4-hydroxy-cyclohept-2-enyl]-2-nitro-benzenesulfonamide

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Chemical Property of N-but-3-enyl-N-[6-(tert-butyl-dimethyl-silanyloxy)-4-hydroxy-cyclohept-2-enyl]-2-nitro-benzenesulfonamide

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Technology Process of N-but-3-enyl-N-[6-(tert-butyl-dimethyl-silanyloxy)-4-hydroxy-cyclohept-2-enyl]-2-nitro-benzenesulfonamide

There total 3 articles about N-but-3-enyl-N-[6-(tert-butyl-dimethyl-silanyloxy)-4-hydroxy-cyclohept-2-enyl]-2-nitro-benzenesulfonamide 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: 96.0%

: 482376-66-9
(-)-(1S,3S,5S)-5-[N-(but-3-enyl)-N-(2-nitrobenzenesulfonyl)amino]-3-(tert-butyl-dimethylsilanyloxy)cyclohept-6-enyl acetate

: 482376-67-0
N-but-3-enyl-N-[6-(tert-butyl-dimethyl-silanyloxy)-4-hydroxy-cyclohept-2-enyl]-2-nitro-benzenesulfonamide

Guidance literature:: With methanol; potassium cyanide; at 20 ℃; for 15h;
DOI:10.1002/1099-0690(200208)2002:16<2855::AID-EJOC2855>3.0.CO;2-1

Reference yield:

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

: 482376-67-0
N-but-3-enyl-N-[6-(tert-butyl-dimethyl-silanyloxy)-4-hydroxy-cyclohept-2-enyl]-2-nitro-benzenesulfonamide

Guidance literature:: Multi-step reaction with 2 steps

1: 89 percent / EtOOC-N=N-COOEt; Ph₃P / tetrahydrofuran / 18 h / 20 °C

2: 96 percent / KCN; MeOH / 15 h / 20 °C

With methanol; potassium cyanide; triphenylphosphine; diethylazodicarboxylate; In tetrahydrofuran; 1: Mitsunobu reaction;
DOI:10.1002/1099-0690(200208)2002:16<2855::AID-EJOC2855>3.0.CO;2-1

Reference yield:

: 134734-52-4
(1R,4S,6S)-4-acetoxy-6-[(tert-butyldimethylsilyl)oxy]-2-cyclohepten-1-ol

: 482376-67-0
N-but-3-enyl-N-[6-(tert-butyl-dimethyl-silanyloxy)-4-hydroxy-cyclohept-2-enyl]-2-nitro-benzenesulfonamide

Guidance literature:: Multi-step reaction with 2 steps

1: 89 percent / EtOOC-N=N-COOEt; Ph₃P / tetrahydrofuran / 18 h / 20 °C

2: 96 percent / KCN; MeOH / 15 h / 20 °C

With methanol; potassium cyanide; triphenylphosphine; diethylazodicarboxylate; In tetrahydrofuran; 1: Mitsunobu reaction;
DOI:10.1002/1099-0690(200208)2002:16<2855::AID-EJOC2855>3.0.CO;2-1