(E)-3-[Benzyloxy-(3-oxo-butyryl)-amino]-2-(4-benzyloxy-phenyl)-acrylic acid methyl ester

Base Information

Chemical Name:(E)-3-[Benzyloxy-(3-oxo-butyryl)-amino]-2-(4-benzyloxy-phenyl)-acrylic acid methyl ester
CAS No.:81790-29-6
Molecular Formula:C₂₈H₂₇NO₆
Molecular Weight:473.525
Hs Code.:

Synonyms:(E)-3-[Benzyloxy-(3-oxo-butyryl)-amino]-2-(4-benzyloxy-phenyl)-acrylic acid methyl ester

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Chemical Property of (E)-3-[Benzyloxy-(3-oxo-butyryl)-amino]-2-(4-benzyloxy-phenyl)-acrylic acid methyl ester

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Technology Process of (E)-3-[Benzyloxy-(3-oxo-butyryl)-amino]-2-(4-benzyloxy-phenyl)-acrylic acid methyl ester

There total 5 articles about (E)-3-[Benzyloxy-(3-oxo-butyryl)-amino]-2-(4-benzyloxy-phenyl)-acrylic acid methyl 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:

: 156-38-7
4-hydroxyphenylacetate

: 81790-29-6
(E)-3-[Benzyloxy-(3-oxo-butyryl)-amino]-2-(4-benzyloxy-phenyl)-acrylic acid methyl ester

Guidance literature:: Multi-step reaction with 5 steps

1: BF₃*OEt₂ / 12 h / Ambient temperature

2: anhydrous potassium carbonate / butan-2-one / 24 h / Heating

3: 89 percent / N,N,N',N'-tetramethylethylenediamine / 12 h / 200 °C

4: 100 percent / camphorsulfonic acid (CSA) / benzene / 12 h / Heating

5: 1.) sec-BuLi / 1.) THF, -78 deg C

With N,N,N,N,-tetramethylethylenediamine; camphor-10-sulfonic acid; boron trifluoride diethyl etherate; sec.-butyllithium; potassium carbonate; In butanone; benzene;
DOI:10.1021/jo00136a005

Reference yield:

: 14199-15-6
Methyl 4-hydroxyphenylacetate

: 81790-29-6
(E)-3-[Benzyloxy-(3-oxo-butyryl)-amino]-2-(4-benzyloxy-phenyl)-acrylic acid methyl ester

Guidance literature:: Multi-step reaction with 4 steps

1: anhydrous potassium carbonate / butan-2-one / 24 h / Heating

2: 89 percent / N,N,N',N'-tetramethylethylenediamine / 12 h / 200 °C

3: 100 percent / camphorsulfonic acid (CSA) / benzene / 12 h / Heating

4: 1.) sec-BuLi / 1.) THF, -78 deg C

With N,N,N,N,-tetramethylethylenediamine; camphor-10-sulfonic acid; sec.-butyllithium; potassium carbonate; In butanone; benzene;
DOI:10.1021/jo00136a005

Reference yield:

: 68641-16-7
(4-benzyloxy-phenyl)-acetic acid methyl ester

: 81790-29-6
(E)-3-[Benzyloxy-(3-oxo-butyryl)-amino]-2-(4-benzyloxy-phenyl)-acrylic acid methyl ester

Guidance literature:: Multi-step reaction with 3 steps

1: 89 percent / N,N,N',N'-tetramethylethylenediamine / 12 h / 200 °C

2: 100 percent / camphorsulfonic acid (CSA) / benzene / 12 h / Heating

3: 1.) sec-BuLi / 1.) THF, -78 deg C

With N,N,N,N,-tetramethylethylenediamine; camphor-10-sulfonic acid; sec.-butyllithium; In benzene;
DOI:10.1021/jo00136a005