5-(benzyloxy)-4-bromo-3-(1-(ethoxymethoxy)ethyl)-7-methoxyisobenzofuran-1(3H)-one

Base Information

Chemical Name:5-(benzyloxy)-4-bromo-3-(1-(ethoxymethoxy)ethyl)-7-methoxyisobenzofuran-1(3H)-one
CAS No.:1610701-89-7
Molecular Formula:C₂₁H₂₃BrO₆
Molecular Weight:451.314
Hs Code.:

Synonyms:5-(benzyloxy)-4-bromo-3-(1-(ethoxymethoxy)ethyl)-7-methoxyisobenzofuran-1(3H)-one

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Chemical Property of 5-(benzyloxy)-4-bromo-3-(1-(ethoxymethoxy)ethyl)-7-methoxyisobenzofuran-1(3H)-one

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Technology Process of 5-(benzyloxy)-4-bromo-3-(1-(ethoxymethoxy)ethyl)-7-methoxyisobenzofuran-1(3H)-one

There total 7 articles about 5-(benzyloxy)-4-bromo-3-(1-(ethoxymethoxy)ethyl)-7-methoxyisobenzofuran-1(3H)-one 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%

: 1610701-84-2
5-(benzyloxy)-3-(1-((tert-butyldimethylsilyl)oxy)ethyl)-7-methoxyisobenzofuran-1(3H)-one

: 1610701-89-7
5-(benzyloxy)-4-bromo-3-(1-(ethoxymethoxy)ethyl)-7-methoxyisobenzofuran-1(3H)-one

Guidance literature:: With N-Bromosuccinimide; In dichloromethane; at 0 - 20 ℃; for 16h; regioselective reaction; Inert atmosphere;
DOI:10.1021/jo5008527

Reference yield:

: 185038-86-2
4-Benzyloxy-2-methoxy-6-trifluoromethanesulfonyloxy-benzoic acid methyl ester

: 1610701-89-7
5-(benzyloxy)-4-bromo-3-(1-(ethoxymethoxy)ethyl)-7-methoxyisobenzofuran-1(3H)-one

Guidance literature:: Multi-step reaction with 5 steps

1: lithium chloride; tetrakis(triphenylphosphine) palladium⁽⁰⁾ / tetrahydrofuran / 48 h / 80 °C / Inert atmosphere

2: potassium tert-butylate / tetrahydrofuran / 24 h / 45 °C / Inert atmosphere

3: osmium(VIII) oxide; 4-methylmorpholine N-oxide / acetone; water; tert-butyl alcohol / 16 h / 20 °C / Inert atmosphere

4: N-ethyl-N,N-diisopropylamine; dmap / tetrahydrofuran; dichloromethane / 48 h / 0 - 20 °C / Inert atmosphere

5: N-Bromosuccinimide / dichloromethane / 16 h / 0 - 20 °C / Inert atmosphere

With dmap; N-Bromosuccinimide; osmium(VIII) oxide; tetrakis(triphenylphosphine) palladium⁽⁰⁾; potassium tert-butylate; 4-methylmorpholine N-oxide; N-ethyl-N,N-diisopropylamine; lithium chloride; In tetrahydrofuran; dichloromethane; water; acetone; tert-butyl alcohol; 1: |Stille Cross Coupling;
DOI:10.1021/jo5008527

Reference yield:

: 83-30-7
acide 2,4,6-trihydroxybenzoique

: 1610701-89-7
5-(benzyloxy)-4-bromo-3-(1-(ethoxymethoxy)ethyl)-7-methoxyisobenzofuran-1(3H)-one

Guidance literature:: Multi-step reaction with 6 steps

1.1: dimethyl sulfate; potassium carbonate / acetone / 16 h / 20 °C / Inert atmosphere

1.2: 3 h / Inert atmosphere; Reflux

2.1: lithium chloride; tetrakis(triphenylphosphine) palladium⁽⁰⁾ / tetrahydrofuran / 48 h / 80 °C / Inert atmosphere

3.1: potassium tert-butylate / tetrahydrofuran / 24 h / 45 °C / Inert atmosphere

4.1: osmium(VIII) oxide; 4-methylmorpholine N-oxide / acetone; water; tert-butyl alcohol / 16 h / 20 °C / Inert atmosphere

5.1: N-ethyl-N,N-diisopropylamine; dmap / tetrahydrofuran; dichloromethane / 48 h / 0 - 20 °C / Inert atmosphere

6.1: N-Bromosuccinimide / dichloromethane / 16 h / 0 - 20 °C / Inert atmosphere

With dmap; N-Bromosuccinimide; osmium(VIII) oxide; tetrakis(triphenylphosphine) palladium⁽⁰⁾; potassium tert-butylate; potassium carbonate; 4-methylmorpholine N-oxide; N-ethyl-N,N-diisopropylamine; dimethyl sulfate; lithium chloride; In tetrahydrofuran; dichloromethane; water; acetone; tert-butyl alcohol; 2.1: |Stille Cross Coupling;
DOI:10.1021/jo5008527