5-(tert-butyl-dimethyl-silanyloxy)-3-(4-methoxy-benzyloxy)-pentanoic acid ethyl ester

Base Information

Chemical Name:5-(tert-butyl-dimethyl-silanyloxy)-3-(4-methoxy-benzyloxy)-pentanoic acid ethyl ester
CAS No.:251641-41-5
Molecular Formula:C₂₁H₃₆O₅Si
Molecular Weight:396.599
Hs Code.:

5-(<i>tert</i>-butyl-dimethyl-silanyloxy)-3-(4-methoxy-benzyloxy)-pentanoic acid ethyl ester

Synonyms:5-(tert-butyl-dimethyl-silanyloxy)-3-(4-methoxy-benzyloxy)-pentanoic acid ethyl ester

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Chemical Property of 5-(tert-butyl-dimethyl-silanyloxy)-3-(4-methoxy-benzyloxy)-pentanoic acid ethyl ester

Chemical Property:

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Technology Process of 5-(tert-butyl-dimethyl-silanyloxy)-3-(4-methoxy-benzyloxy)-pentanoic acid ethyl ester

There total 4 articles about 5-(tert-butyl-dimethyl-silanyloxy)-3-(4-methoxy-benzyloxy)-pentanoic acid ethyl ester 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:

: 113335-04-9
(R)-5-Benzyloxy-3-hydroxy-pentanoic acid ethyl ester

: 251641-41-5
5-(tert-butyl-dimethyl-silanyloxy)-3-(4-methoxy-benzyloxy)-pentanoic acid ethyl ester

Guidance literature:: Multi-step reaction with 3 steps

1: H₂ / Pd/C / ethanol

2: imidazole / tetrahydrofuran / 0 °C

3: BF₃*OEt₂ / CH₂Cl₂

With 1H-imidazole; boron trifluoride diethyl etherate; hydrogen; palladium on activated charcoal; In tetrahydrofuran; ethanol; dichloromethane; 1: Hydrogenation / 2: silylation / 3: Alkylation;
DOI:10.1021/jo9910987

Reference yield:

: 18162-48-6
tert-butyldimethylsilyl chloride

: 251641-41-5
5-(tert-butyl-dimethyl-silanyloxy)-3-(4-methoxy-benzyloxy)-pentanoic acid ethyl ester

Guidance literature:: Multi-step reaction with 2 steps

1: imidazole / tetrahydrofuran / 0 °C

2: BF₃*OEt₂ / CH₂Cl₂

With 1H-imidazole; boron trifluoride diethyl etherate; In tetrahydrofuran; dichloromethane; 1: silylation / 2: Alkylation;
DOI:10.1021/jo9910987

Reference yield:

: (R)-3,5-Dihydroxy-pentanoic acid ethyl ester

: 251641-41-5
5-(tert-butyl-dimethyl-silanyloxy)-3-(4-methoxy-benzyloxy)-pentanoic acid ethyl ester

Guidance literature:: Multi-step reaction with 2 steps

1: imidazole / tetrahydrofuran / 0 °C

2: BF₃*OEt₂ / CH₂Cl₂

With 1H-imidazole; boron trifluoride diethyl etherate; In tetrahydrofuran; dichloromethane; 1: silylation / 2: Alkylation;
DOI:10.1021/jo9910987