[4-(Benzyloxycarbonylamino-methyl)-2-methoxy-phenoxy]-acetic Acid Methyl Ester

Base Information

Chemical Name:[4-(Benzyloxycarbonylamino-methyl)-2-methoxy-phenoxy]-acetic Acid Methyl Ester
CAS No.:289903-31-7
Molecular Formula:C₁₉H₂₁NO₆
Molecular Weight:359.379
Hs Code.:

Synonyms:[4-(Benzyloxycarbonylamino-methyl)-2-methoxy-phenoxy]-acetic Acid Methyl Ester

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Chemical Property of [4-(Benzyloxycarbonylamino-methyl)-2-methoxy-phenoxy]-acetic Acid Methyl Ester

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Technology Process of [4-(Benzyloxycarbonylamino-methyl)-2-methoxy-phenoxy]-acetic Acid Methyl Ester

There total 5 articles about [4-(Benzyloxycarbonylamino-methyl)-2-methoxy-phenoxy]-acetic 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: 90.0%

: 96-32-2
bromoacetic acid methyl ester

: 289903-29-3
benzyl N-(4-hydroxy-3-methoxybenzyl)carbamate

: 289903-31-7
[4-(Benzyloxycarbonylamino-methyl)-2-methoxy-phenoxy]-acetic Acid Methyl Ester

Guidance literature:: With potassium carbonate; In acetone; for 3h; Heating;
DOI:10.1016/S0968-0896(01)00387-X

Reference yield:

: 4421-08-3
3-methoxy-4-hydroxybenzonitrile

: 289903-31-7
[4-(Benzyloxycarbonylamino-methyl)-2-methoxy-phenoxy]-acetic Acid Methyl Ester

Guidance literature:: Multi-step reaction with 5 steps

1: 92 percent / diisopropylethylamine / CH₂Cl₂ / 3 h / 20 °C

2: lithium aluminum hydride / tetrahydrofuran / 4 h / Heating

3: 8.28 g / triethylamine / CH₂Cl₂ / 2 h / 20 °C

4: 95 percent / trifluoroacetic acid / CH₂Cl₂ / 0.17 h / 20 °C

5: 90 percent / potassium carbonate / acetone / 3 h / Heating

With lithium aluminium tetrahydride; potassium carbonate; triethylamine; N-ethyl-N,N-diisopropylamine; trifluoroacetic acid; In tetrahydrofuran; dichloromethane; acetone;
DOI:10.1016/S0968-0896(01)00387-X

Reference yield:

: 161196-85-6
3-methoxy-4-(methoxymethyloxy)benzonitrile

: 289903-31-7
[4-(Benzyloxycarbonylamino-methyl)-2-methoxy-phenoxy]-acetic Acid Methyl Ester

Guidance literature:: Multi-step reaction with 4 steps

1: lithium aluminum hydride / tetrahydrofuran / 4 h / Heating

2: 8.28 g / triethylamine / CH₂Cl₂ / 2 h / 20 °C

3: 95 percent / trifluoroacetic acid / CH₂Cl₂ / 0.17 h / 20 °C

4: 90 percent / potassium carbonate / acetone / 3 h / Heating

With lithium aluminium tetrahydride; potassium carbonate; triethylamine; trifluoroacetic acid; In tetrahydrofuran; dichloromethane; acetone;
DOI:10.1016/S0968-0896(01)00387-X