8-t-butyldimethylsilyloxy-3-(1-cyano-2-phenyl)ethyl-6-methoxy-1-oxo-1H-2-benzopyran

Base Information

Chemical Name:8-t-butyldimethylsilyloxy-3-(1-cyano-2-phenyl)ethyl-6-methoxy-1-oxo-1H-2-benzopyran
CAS No.:342906-14-3
Molecular Formula:C₂₅H₂₉NO₄Si
Molecular Weight:435.595
Hs Code.:

Synonyms:8-t-butyldimethylsilyloxy-3-(1-cyano-2-phenyl)ethyl-6-methoxy-1-oxo-1H-2-benzopyran

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Chemical Property of 8-t-butyldimethylsilyloxy-3-(1-cyano-2-phenyl)ethyl-6-methoxy-1-oxo-1H-2-benzopyran

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Technology Process of 8-t-butyldimethylsilyloxy-3-(1-cyano-2-phenyl)ethyl-6-methoxy-1-oxo-1H-2-benzopyran

There total 4 articles about 8-t-butyldimethylsilyloxy-3-(1-cyano-2-phenyl)ethyl-6-methoxy-1-oxo-1H-2-benzopyran 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: 20.0%

: 100-39-0
benzyl bromide

: 181427-91-8
8-t-butyldimethylsilyloxy-3-cyanomethyl-6-methoxy-1-oxo-1H-2-benzopyran

: 342906-14-3
8-t-butyldimethylsilyloxy-3-(1-cyano-2-phenyl)ethyl-6-methoxy-1-oxo-1H-2-benzopyran

Guidance literature:: With sodium hydroxide; tetrabutylammomium bromide; In dichloromethane; water; at 0 ℃;
DOI:10.7164/antibiotics.54.285

Reference yield:

: 132971-59-6
8-hydroxy-3-hydroxymethyl-6-methoxyisocoumarin

: 342906-14-3
8-t-butyldimethylsilyloxy-3-(1-cyano-2-phenyl)ethyl-6-methoxy-1-oxo-1H-2-benzopyran

Guidance literature:: Multi-step reaction with 4 steps

1: 88 percent / CCl₄; PPh₃ / tetrahydrofuran / 2 h / Heating

2: 84 percent / dimethylsulfoxide / 1 h / 20 °C

3: 75 percent / imidazole / dimethylformamide / 2 h / 0 °C

4: 20 percent / NaOH; tetra-n-butyl ammonium bromide / CH₂Cl₂; H₂O / 0 °C

With 1H-imidazole; tetrachloromethane; sodium hydroxide; tetrabutylammomium bromide; triphenylphosphine; In tetrahydrofuran; dichloromethane; water; dimethyl sulfoxide; N,N-dimethyl-formamide;
DOI:10.7164/antibiotics.54.285

Reference yield:

: 149457-12-5
3-chloromethyl-8-hydroxy-6-methoxy-1-oxo-1H-2-benzopyran

: 342906-14-3
8-t-butyldimethylsilyloxy-3-(1-cyano-2-phenyl)ethyl-6-methoxy-1-oxo-1H-2-benzopyran

Guidance literature:: Multi-step reaction with 3 steps

1: 84 percent / dimethylsulfoxide / 1 h / 20 °C

2: 75 percent / imidazole / dimethylformamide / 2 h / 0 °C

3: 20 percent / NaOH; tetra-n-butyl ammonium bromide / CH₂Cl₂; H₂O / 0 °C

With 1H-imidazole; sodium hydroxide; tetrabutylammomium bromide; In dichloromethane; water; dimethyl sulfoxide; N,N-dimethyl-formamide;
DOI:10.7164/antibiotics.54.285