4-(tert-butoxycarbonylamino)-2-(4-(triisopropylsilyloxy)phenyl)butanoic acid

Base Information

Chemical Name:4-(tert-butoxycarbonylamino)-2-(4-(triisopropylsilyloxy)phenyl)butanoic acid
CAS No.:1253955-47-3
Molecular Formula:C₂₄H₄₁NO₅Si
Molecular Weight:451.679
Hs Code.:

Synonyms:4-(tert-butoxycarbonylamino)-2-(4-(triisopropylsilyloxy)phenyl)butanoic acid

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Chemical Property of 4-(tert-butoxycarbonylamino)-2-(4-(triisopropylsilyloxy)phenyl)butanoic acid

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Technology Process of 4-(tert-butoxycarbonylamino)-2-(4-(triisopropylsilyloxy)phenyl)butanoic acid

There total 4 articles about 4-(tert-butoxycarbonylamino)-2-(4-(triisopropylsilyloxy)phenyl)butanoic 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:

: 1253955-46-2
benzyl 4-(tertbutoxycarbonylamino)-2-(4-(triisopropylsilyloxy)phenyl)butanoate

: 1253955-47-3
4-(tert-butoxycarbonylamino)-2-(4-(triisopropylsilyloxy)phenyl)butanoic acid

Guidance literature:: With hydrogen; palladium 10% on activated carbon; In ethyl acetate; for 2h;

Reference yield:

: 27727-37-3
benzyl p-hydroxyphenylacetate

: 1253955-47-3
4-(tert-butoxycarbonylamino)-2-(4-(triisopropylsilyloxy)phenyl)butanoic acid

Guidance literature:: Multi-step reaction with 4 steps

1.1: 2,6-dimethylpyridine / dichloromethane / 2.5 h / 0 °C

2.1: lithium hexamethyldisilazane / tetrahydrofuran / 0.5 h / -78 °C

2.2: 2 h / -78 - 0 °C

3.1: cobalt(II) chloride hexahydrate; sodium tetrahydroborate / methanol / 0.33 h / 0 °C

3.2: 0.33 h / 0 °C

3.3: 1.5 h / 0 °C

4.1: palladium 10% on activated carbon; hydrogen / ethyl acetate / 2 h

With 2,6-dimethylpyridine; sodium tetrahydroborate; cobalt(II) chloride hexahydrate; palladium 10% on activated carbon; hydrogen; lithium hexamethyldisilazane; In tetrahydrofuran; methanol; dichloromethane; ethyl acetate;

Reference yield:

: 1253955-44-0
benzyl 2-(4-(triisopropylsiloxy)phenyl)acetate

: 1253955-47-3
4-(tert-butoxycarbonylamino)-2-(4-(triisopropylsilyloxy)phenyl)butanoic acid

Guidance literature:: Multi-step reaction with 3 steps

1.1: lithium hexamethyldisilazane / tetrahydrofuran / 0.5 h / -78 °C

1.2: 2 h / -78 - 0 °C

2.1: cobalt(II) chloride hexahydrate; sodium tetrahydroborate / methanol / 0.33 h / 0 °C

2.2: 0.33 h / 0 °C

2.3: 1.5 h / 0 °C

3.1: palladium 10% on activated carbon; hydrogen / ethyl acetate / 2 h

With sodium tetrahydroborate; cobalt(II) chloride hexahydrate; palladium 10% on activated carbon; hydrogen; lithium hexamethyldisilazane; In tetrahydrofuran; methanol; ethyl acetate;