(4-{[4-(tert-butyl-dimethyl-silanyloxy)-phenyl]-acetoxy}-phenyl)-acetic acid

Base Information

Chemical Name:(4-{[4-(tert-butyl-dimethyl-silanyloxy)-phenyl]-acetoxy}-phenyl)-acetic acid
CAS No.:423157-93-1
Molecular Formula:C₂₂H₂₈O₅Si
Molecular Weight:400.547
Hs Code.:

(4-{[4-(<i>tert</i>-butyl-dimethyl-silanyloxy)-phenyl]-acetoxy}-phenyl)-acetic acid

Synonyms:(4-{[4-(tert-butyl-dimethyl-silanyloxy)-phenyl]-acetoxy}-phenyl)-acetic acid

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Chemical Property of (4-{[4-(tert-butyl-dimethyl-silanyloxy)-phenyl]-acetoxy}-phenyl)-acetic acid

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Technology Process of (4-{[4-(tert-butyl-dimethyl-silanyloxy)-phenyl]-acetoxy}-phenyl)-acetic acid

There total 5 articles about (4-{[4-(tert-butyl-dimethyl-silanyloxy)-phenyl]-acetoxy}-phenyl)-acetic acid 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: 99.0%

: 335200-37-8
[4-(tert-butyl-dimethyl-silanyloxy)-phenyl]-acetic acid 4-benzyloxycarbonylmethyl-phenyl ester

: 423157-93-1
(4-{[4-(tert-butyl-dimethyl-silanyloxy)-phenyl]-acetoxy}-phenyl)-acetic acid

Guidance literature:: With hydrogen; palladium on activated charcoal; In methanol; ethyl acetate; for 2h;
DOI:10.1039/b008065i

Reference yield:

: 156-38-7
4-hydroxyphenylacetate

: 423157-93-1
(4-{[4-(tert-butyl-dimethyl-silanyloxy)-phenyl]-acetoxy}-phenyl)-acetic acid

Guidance literature:: Multi-step reaction with 3 steps

1: 75 percent / 1,8-diazabicyclo[5.4.0]undec-7-ene / acetonitrile / 16 °C / Heating

2: 76 percent / 1-(3-dimethylaminopropyl)-3-ethylcarbodiimide hydrochloride; 1-hydroxybenzotriazole hydrate; N,N-diisopropylethylamine / tetrahydrofuran / 2 h / 20 °C

3: 99 percent / H₂ / Pd/C / methanol; ethyl acetate / 2 h

With hydrogen; 1,8-diazabicyclo[5.4.0]undec-7-ene; 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride; palladium on activated charcoal; In tetrahydrofuran; methanol; ethyl acetate; acetonitrile;
DOI:10.1039/b008065i

Reference yield:

: 27727-37-3
benzyl p-hydroxyphenylacetate

: 423157-93-1
(4-{[4-(tert-butyl-dimethyl-silanyloxy)-phenyl]-acetoxy}-phenyl)-acetic acid

Guidance literature:: Multi-step reaction with 2 steps

1: 76 percent / 1-(3-dimethylaminopropyl)-3-ethylcarbodiimide hydrochloride; 1-hydroxybenzotriazole hydrate; N,N-diisopropylethylamine / tetrahydrofuran / 2 h / 20 °C

2: 99 percent / H₂ / Pd/C / methanol; ethyl acetate / 2 h

With hydrogen; 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride; palladium on activated charcoal; In tetrahydrofuran; methanol; ethyl acetate;
DOI:10.1039/b008065i