((1R,2S,3R,4S)-3-Benzenesulfonyl-bicyclo[2.2.1]hept-5-en-2-yl)-trimethyl-silane

Base Information

Chemical Name:((1R,2S,3R,4S)-3-Benzenesulfonyl-bicyclo[2.2.1]hept-5-en-2-yl)-trimethyl-silane
CAS No.:82262-89-3
Molecular Formula:C₁₆H₂₂O₂SSi
Molecular Weight:306.501
Hs Code.:

Synonyms:((1R,2S,3R,4S)-3-Benzenesulfonyl-bicyclo[2.2.1]hept-5-en-2-yl)-trimethyl-silane

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Chemical Property of ((1R,2S,3R,4S)-3-Benzenesulfonyl-bicyclo[2.2.1]hept-5-en-2-yl)-trimethyl-silane

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Technology Process of ((1R,2S,3R,4S)-3-Benzenesulfonyl-bicyclo[2.2.1]hept-5-en-2-yl)-trimethyl-silane

There total 2 articles about ((1R,2S,3R,4S)-3-Benzenesulfonyl-bicyclo[2.2.1]hept-5-en-2-yl)-trimethyl-silane 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: 58.0%

: 64489-07-2
cis-1-(phenylsulfonyl)-2-(trimethylsilyl)ethylene

: 542-92-7,25568-84-7,7313-32-8
cyclopenta-1,3-diene

: 82262-89-3
((1R,2S,3R,4S)-3-Benzenesulfonyl-bicyclo[2.2.1]hept-5-en-2-yl)-trimethyl-silane

Guidance literature:: In benzene; at 55 ℃; for 84h;
DOI:10.1021/jo00173a039

Reference yield:

: 32501-93-2
1-(Phenylsulfonyl)-2-(trimethylsilyl)acetylene

: 82262-89-3
((1R,2S,3R,4S)-3-Benzenesulfonyl-bicyclo[2.2.1]hept-5-en-2-yl)-trimethyl-silane

Guidance literature:: Multi-step reaction with 2 steps

1: 35 percent / H₂ / 5percent Pd/C / ethyl acetate; pyridine / 4.5 h / 2585.7 Torr

2: 58 percent / benzene / 84 h / 55 °C

With hydrogen; palladium on activated charcoal; In pyridine; ethyl acetate; benzene;
DOI:10.1021/jo00173a039

Reference yield:

: 82262-89-3
((1R,2S,3R,4S)-3-Benzenesulfonyl-bicyclo[2.2.1]hept-5-en-2-yl)-trimethyl-silane

: 10211-14-0
C₂₇H₂₂O

Guidance literature:: Multi-step reaction with 2 steps

1: 30 mg / benzene / 60 h / Heating

2: 72 percent / 1M tetra-n-butylammonium fluoride / tetrahydrofuran / 3.5 h / Heating

With tetrabutyl ammonium fluoride; In tetrahydrofuran; benzene;
DOI:10.1021/jo00173a039