[(6-Benzyloxy-benzo[1,3]dioxol-5-yl)-(3,4,5-trimethoxy-phenyl)-methyl]-carbamic acid 2-hydroxy-ethyl ester

Base Information

Chemical Name:[(6-Benzyloxy-benzo[1,3]dioxol-5-yl)-(3,4,5-trimethoxy-phenyl)-methyl]-carbamic acid 2-hydroxy-ethyl ester
CAS No.:161234-78-2
Molecular Formula:C₂₇H₂₉NO₉
Molecular Weight:511.529
Hs Code.:

Synonyms:[(6-Benzyloxy-benzo[1,3]dioxol-5-yl)-(3,4,5-trimethoxy-phenyl)-methyl]-carbamic acid 2-hydroxy-ethyl ester

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Chemical Property of [(6-Benzyloxy-benzo[1,3]dioxol-5-yl)-(3,4,5-trimethoxy-phenyl)-methyl]-carbamic acid 2-hydroxy-ethyl ester

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Technology Process of [(6-Benzyloxy-benzo[1,3]dioxol-5-yl)-(3,4,5-trimethoxy-phenyl)-methyl]-carbamic acid 2-hydroxy-ethyl ester

There total 6 articles about [(6-Benzyloxy-benzo[1,3]dioxol-5-yl)-(3,4,5-trimethoxy-phenyl)-methyl]-carbamic acid 2-hydroxy-ethyl 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: 98.0%

: 161234-77-1
3-[(6-Benzyloxy-benzo[1,3]dioxol-5-yl)-(3,4,5-trimethoxy-phenyl)-methyl]-oxazolidine-2,4-dione

: 161234-78-2
[(6-Benzyloxy-benzo[1,3]dioxol-5-yl)-(3,4,5-trimethoxy-phenyl)-methyl]-carbamic acid 2-hydroxy-ethyl ester

Guidance literature:: With sodium tetrahydroborate; In tetrahydrofuran; ethanol; water;
DOI:10.1016/S0040-4039(00)78553-4

Reference yield:

: 533-31-3
Sesamol

: 161234-78-2
[(6-Benzyloxy-benzo[1,3]dioxol-5-yl)-(3,4,5-trimethoxy-phenyl)-methyl]-carbamic acid 2-hydroxy-ethyl ester

Guidance literature:: Multi-step reaction with 5 steps

1: K₂CO₃ / acetone

2: Br₂, AcONa / acetic acid

3: 88 percent / n-BuLi / tetrahydrofuran / -45 °C

4: 87 percent / triphenylphosphine, diethyl azodicarboxylate / tetrahydrofuran / 12 h / Ambient temperature

5: 98 percent / NaBH₄ / tetrahydrofuran; H₂O; ethanol

With sodium tetrahydroborate; n-butyllithium; bromine; sodium acetate; potassium carbonate; triphenylphosphine; diethylazodicarboxylate; In tetrahydrofuran; ethanol; water; acetic acid; acetone;
DOI:10.1016/S0040-4039(00)78553-4

Reference yield:

: 66177-24-0
5-(benzyloxy)benzo[d][1,3]dioxole

: 161234-78-2
[(6-Benzyloxy-benzo[1,3]dioxol-5-yl)-(3,4,5-trimethoxy-phenyl)-methyl]-carbamic acid 2-hydroxy-ethyl ester

Guidance literature:: Multi-step reaction with 4 steps

1: Br₂, AcONa / acetic acid

2: 88 percent / n-BuLi / tetrahydrofuran / -45 °C

3: 87 percent / triphenylphosphine, diethyl azodicarboxylate / tetrahydrofuran / 12 h / Ambient temperature

4: 98 percent / NaBH₄ / tetrahydrofuran; H₂O; ethanol

With sodium tetrahydroborate; n-butyllithium; bromine; sodium acetate; triphenylphosphine; diethylazodicarboxylate; In tetrahydrofuran; ethanol; water; acetic acid;
DOI:10.1016/S0040-4039(00)78553-4