ethyl 4-cyano-4-(3,4-dichloro-phenyl)-6-(t-butyldimethylsilyloxy)-hexanoate

Base Information

Chemical Name:ethyl 4-cyano-4-(3,4-dichloro-phenyl)-6-(t-butyldimethylsilyloxy)-hexanoate
CAS No.:178371-52-3
Molecular Formula:C₂₁H₃₁Cl₂NO₃Si
Molecular Weight:444.474
Hs Code.:

Synonyms:ethyl 4-cyano-4-(3,4-dichloro-phenyl)-6-(t-butyldimethylsilyloxy)-hexanoate

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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 ethyl 4-cyano-4-(3,4-dichloro-phenyl)-6-(t-butyldimethylsilyloxy)-hexanoate

Chemical Property:

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Technology Process of ethyl 4-cyano-4-(3,4-dichloro-phenyl)-6-(t-butyldimethylsilyloxy)-hexanoate

There total 5 articles about ethyl 4-cyano-4-(3,4-dichloro-phenyl)-6-(t-butyldimethylsilyloxy)-hexanoate 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:

: 191604-24-7
2-(3,4-dichloro-phenyl)-4-(t-butyldimethylsilyloxy)-butyronitrile

: 539-74-2
Ethyl 3-bromopropionate

: 178371-52-3
ethyl 4-cyano-4-(3,4-dichloro-phenyl)-6-(t-butyldimethylsilyloxy)-hexanoate

Guidance literature:: With lithium hexamethyldisilazane; In tetrahydrofuran; water;

Reference yield:

: 191604-24-7
2-(3,4-dichloro-phenyl)-4-(t-butyldimethylsilyloxy)-butyronitrile

: 539-74-2
Ethyl 3-bromopropionate

: 4039-32-1
lithium hexamethyldisilazane

: 178371-52-3
ethyl 4-cyano-4-(3,4-dichloro-phenyl)-6-(t-butyldimethylsilyloxy)-hexanoate

Guidance literature:: In tetrahydrofuran; water;

Reference yield:

: 86864-60-0
2-(tert-butyldimethylsilyloxy)ethyl bromide

: 178371-52-3
ethyl 4-cyano-4-(3,4-dichloro-phenyl)-6-(t-butyldimethylsilyloxy)-hexanoate

Guidance literature:: Multi-step reaction with 2 steps

1: hydrogenchloride / tetrahydrofuran

2: tetrahydrofuran; water

With hydrogenchloride; In tetrahydrofuran; water;