{4-[2-(4-Acetylamino-phenyl)-acetoxy]-phenyl}-acetic acid 4-benzyloxycarbonylmethyl-phenyl ester

Base Information

Chemical Name:{4-[2-(4-Acetylamino-phenyl)-acetoxy]-phenyl}-acetic acid 4-benzyloxycarbonylmethyl-phenyl ester
CAS No.:335200-41-4
Molecular Formula:C₃₃H₂₉NO₇
Molecular Weight:551.596
Hs Code.:

Synonyms:{4-[2-(4-Acetylamino-phenyl)-acetoxy]-phenyl}-acetic acid 4-benzyloxycarbonylmethyl-phenyl ester

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Chemical Property of {4-[2-(4-Acetylamino-phenyl)-acetoxy]-phenyl}-acetic acid 4-benzyloxycarbonylmethyl-phenyl ester

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Technology Process of {4-[2-(4-Acetylamino-phenyl)-acetoxy]-phenyl}-acetic acid 4-benzyloxycarbonylmethyl-phenyl ester

There total 5 articles about {4-[2-(4-Acetylamino-phenyl)-acetoxy]-phenyl}-acetic acid 4-benzyloxycarbonylmethyl-phenyl 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: 93.0%

: 27727-37-3
benzyl p-hydroxyphenylacetate

: 335200-30-1
{4-[2-(4-Acetylamino-phenyl)-acetoxy]-phenyl}-acetic acid

: 335200-41-4
{4-[2-(4-Acetylamino-phenyl)-acetoxy]-phenyl}-acetic acid 4-benzyloxycarbonylmethyl-phenyl ester

Guidance literature:: With 1-hydroxybenzotriazol-hydrate; 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride; N-ethyl-N,N-diisopropylamine; In tetrahydrofuran; for 3h;
DOI:10.1039/b008065i

Reference yield:

: 156-38-7
4-hydroxyphenylacetate

: 335200-41-4
{4-[2-(4-Acetylamino-phenyl)-acetoxy]-phenyl}-acetic acid 4-benzyloxycarbonylmethyl-phenyl ester

Guidance literature:: Multi-step reaction with 4 steps

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

2: 90 percent / 1-(3-dimethylaminopropyl)-3-ethylcarbodiimide hydrochloride; 1-hydroxybenzotriazole hydrate; N,N-diisopropylethylamine / tetrahydrofuran / 4 h / 20 °C

3: 95 percent / H₂ / Pd/C / methanol / 2 h

4: 93 percent / 1-(3-dimethylaminopropyl)-3-ethylcarbodiimide hydrochloride; 1-hydroxybenzotriazole hydrate; N,N-diisopropylethylamine / tetrahydrofuran / 3 h

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

Reference yield:

: 335200-40-3
(4-acetylamino-phenyl)-acetic acid 4-benzyloxycarbonylmethyl-phenyl ester

: 335200-41-4
{4-[2-(4-Acetylamino-phenyl)-acetoxy]-phenyl}-acetic acid 4-benzyloxycarbonylmethyl-phenyl ester

Guidance literature:: Multi-step reaction with 2 steps

1: 95 percent / H₂ / Pd/C / methanol / 2 h

2: 93 percent / 1-(3-dimethylaminopropyl)-3-ethylcarbodiimide hydrochloride; 1-hydroxybenzotriazole hydrate; N,N-diisopropylethylamine / tetrahydrofuran / 3 h

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