7-benzyloxy-3-(tert-butyl-dimethyl-silanyloxymethyl)-3-hydroxymethyl-3H-isobenzofuran-1-one

Base Information

Chemical Name:7-benzyloxy-3-(tert-butyl-dimethyl-silanyloxymethyl)-3-hydroxymethyl-3H-isobenzofuran-1-one
CAS No.:721449-05-4
Molecular Formula:C₂₃H₃₀O₅Si
Molecular Weight:414.574
Hs Code.:

7-benzyloxy-3-(<i>tert</i>-butyl-dimethyl-silanyloxymethyl)-3-hydroxymethyl-3<i>H</i>-isobenzofuran-1-one

Synonyms:7-benzyloxy-3-(tert-butyl-dimethyl-silanyloxymethyl)-3-hydroxymethyl-3H-isobenzofuran-1-one

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Chemical Property of 7-benzyloxy-3-(tert-butyl-dimethyl-silanyloxymethyl)-3-hydroxymethyl-3H-isobenzofuran-1-one

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Technology Process of 7-benzyloxy-3-(tert-butyl-dimethyl-silanyloxymethyl)-3-hydroxymethyl-3H-isobenzofuran-1-one

There total 6 articles about 7-benzyloxy-3-(tert-butyl-dimethyl-silanyloxymethyl)-3-hydroxymethyl-3H-isobenzofuran-1-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:

: 18162-48-6
tert-butyldimethylsilyl chloride

: 721448-93-7
7-benzyloxy-3,3-bis-hydroxymethyl-3H-isobenzofuran-1-one

: 721449-05-4
7-benzyloxy-3-(tert-butyl-dimethyl-silanyloxymethyl)-3-hydroxymethyl-3H-isobenzofuran-1-one

: 721449-06-5
7-benzyloxy-3-(tert-butyl-dimethyl-silanyloxymethyl)-3-hydroxymethyl-3H-isobenzofuran-1-one

Guidance literature:: With 1H-imidazole; In N,N-dimethyl-formamide; at 0 ℃; for 2h;
DOI:10.1016/j.bmcl.2004.02.097

Reference yield:

: 19311-91-2
N,N-diethylsalicylamide

: 721449-05-4
7-benzyloxy-3-(tert-butyl-dimethyl-silanyloxymethyl)-3-hydroxymethyl-3H-isobenzofuran-1-one

Guidance literature:: Multi-step reaction with 6 steps

1.1: 100 percent / Et₃N; DMAP / CH₂Cl₂ / 15 h / 20 °C

2.1: s-BuLi; N,N,N',N'-tetramethylethylenediamine / tetrahydrofuran / 1.5 h / -40 °C

2.2: tetrahydrofuran / 17 h / -40 - -30 °C

2.3: NaH / tetrahydrofuran / 3 h / 70 °C

3.1: K₂CO₃ / methanol / 3 h / 70 °C

4.1: 85 percent / K₂CO₃ / acetone / 19 h / 20 °C

5.1: 94 percent / HF*Py / pyridine; CH₂Cl₂ / 20 °C

6.1: imidazole / dimethylformamide / 2 h / 0 °C

With 1H-imidazole; dmap; N,N,N,N,-tetramethylethylenediamine; sec.-butyllithium; potassium carbonate; pyridine hydrogenfluoride; triethylamine; In tetrahydrofuran; pyridine; methanol; dichloromethane; N,N-dimethyl-formamide; acetone;
DOI:10.1016/j.bmcl.2004.02.097

Reference yield:

: 100-39-0
benzyl bromide

: 721449-05-4
7-benzyloxy-3-(tert-butyl-dimethyl-silanyloxymethyl)-3-hydroxymethyl-3H-isobenzofuran-1-one

Guidance literature:: Multi-step reaction with 3 steps

1: 85 percent / K₂CO₃ / acetone / 19 h / 20 °C

2: 94 percent / HF*Py / pyridine; CH₂Cl₂ / 20 °C

3: imidazole / dimethylformamide / 2 h / 0 °C

With 1H-imidazole; potassium carbonate; pyridine hydrogenfluoride; In pyridine; dichloromethane; N,N-dimethyl-formamide; acetone;
DOI:10.1016/j.bmcl.2004.02.097