4-(tert-butyl-dimethyl-silanyloxymethyl)-1-(4-methoxy-phenyl)-hexahydro-pyrano[4,3-d]oxazol-2-one

Base Information

• Chemical Name: 4-(tert-butyl-dimethyl-silanyloxymethyl)-1-(4-methoxy-phenyl)-hexahydro-pyrano[4,3-d]oxazol-2-one
• CAS No.: 413193-52-9
• Molecular Formula: C₂₀H₃₁NO₅Si
• Molecular Weight: 393.555

Synonyms:4-(tert-butyl-dimethyl-silanyloxymethyl)-1-(4-methoxy-phenyl)-hexahydro-pyrano[4,3-d]oxazol-2-one

Chemical Property of 4-(tert-butyl-dimethyl-silanyloxymethyl)-1-(4-methoxy-phenyl)-hexahydro-pyrano[4,3-d]oxazol-2-one

Chemical Property:

Purity/Quality:

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Technology Process of 4-(tert-butyl-dimethyl-silanyloxymethyl)-1-(4-methoxy-phenyl)-hexahydro-pyrano[4,3-d]oxazol-2-one

There total 4 articles about 4-(tert-butyl-dimethyl-silanyloxymethyl)-1-(4-methoxy-phenyl)-hexahydro-pyrano[4,3-d]oxazol-2-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: 87.0%

(4-methoxy-phenyl)-carbamic acid 2-(tert-butyl-dimethyl-silanyloxymethyl)-3,6-dihydro-2H-pyran-3-yl ester (413192-56-0) → 4-(tert-butyl-dimethyl-silanyloxymethyl)-1-(4-methoxy-phenyl)-hexahydro-pyrano[4,3-d]oxazol-2-one (413193-52-9)

Guidance literature:

With sodium hydrogencarbonate; 1-hydroxy-3H-benz[d][1,2]iodoxole-1,3-dione; In tetrahydrofuran; dimethyl sulfoxide; at 90 ℃; for 24h;

DOI:10.1021/ja012126h

Reference yield:

6-O-(tert-butyldimethylsilyl)-1,5-anhydro-2,3-dideoxy-D-erythro-hex-2-enitol (132375-36-1) → 4-(tert-butyl-dimethyl-silanyloxymethyl)-1-(4-methoxy-phenyl)-hexahydro-pyrano[4,3-d]oxazol-2-one (413193-52-9)

Guidance literature:

Multi-step reaction with 2 steps

1: 92 percent / DBU / CH₂Cl₂

2: 87 percent / o-iodoxybenzoic acid; NaHCO₃ / tetrahydrofuran; dimethylsulfoxide / 24 h / 90 °C

With sodium hydrogencarbonate; 1,8-diazabicyclo[5.4.0]undec-7-ene; 1-hydroxy-3H-benz[d][1,2]iodoxole-1,3-dione; In tetrahydrofuran; dichloromethane; dimethyl sulfoxide;

DOI:10.1021/ja012126h

Reference yield:

4-Methoxyphenyl isocyanate (5416-93-3) → 4-(tert-butyl-dimethyl-silanyloxymethyl)-1-(4-methoxy-phenyl)-hexahydro-pyrano[4,3-d]oxazol-2-one (413193-52-9)

Guidance literature:

Multi-step reaction with 2 steps

1: 92 percent / DBU / CH₂Cl₂

2: 87 percent / o-iodoxybenzoic acid; NaHCO₃ / tetrahydrofuran; dimethylsulfoxide / 24 h / 90 °C

With sodium hydrogencarbonate; 1,8-diazabicyclo[5.4.0]undec-7-ene; 1-hydroxy-3H-benz[d][1,2]iodoxole-1,3-dione; In tetrahydrofuran; dichloromethane; dimethyl sulfoxide;

DOI:10.1021/ja012126h

upstream raw materials:

(4-methoxy-phenyl)-carbamic acid 2-(tert-butyl-dimethyl-silanyloxymethyl)-3,6-dihydro-2H-pyran-3-yl ester

6-O-(tert-butyldimethylsilyl)-1,5-anhydro-2,3-dideoxy-D-erythro-hex-2-enitol

4-Methoxyphenyl isocyanate

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