6-({[tert-butyl(diphenyl)silyl]oxy}methyl)-3-(2-hydroxyethyl)-1,3-benzoxazol-2(3H)-one

Base Information

Chemical Name:6-({[tert-butyl(diphenyl)silyl]oxy}methyl)-3-(2-hydroxyethyl)-1,3-benzoxazol-2(3H)-one
CAS No.:1435516-85-0
Molecular Formula:C₂₆H₂₉NO₄Si
Molecular Weight:447.606
Hs Code.:

Synonyms:6-({[tert-butyl(diphenyl)silyl]oxy}methyl)-3-(2-hydroxyethyl)-1,3-benzoxazol-2(3H)-one

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Chemical Property of 6-({[tert-butyl(diphenyl)silyl]oxy}methyl)-3-(2-hydroxyethyl)-1,3-benzoxazol-2(3H)-one

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Technology Process of 6-({[tert-butyl(diphenyl)silyl]oxy}methyl)-3-(2-hydroxyethyl)-1,3-benzoxazol-2(3H)-one

There total 5 articles about 6-({[tert-butyl(diphenyl)silyl]oxy}methyl)-3-(2-hydroxyethyl)-1,3-benzoxazol-2(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: 44.0%

: 1435516-84-9
6-({[tert-butyl(diphenyl)silyl]oxy}methyl)-1,3-benzoxazol-2(3H)-one

: 540-51-2
2-bromoethanol

: 1435516-85-0
6-({[tert-butyl(diphenyl)silyl]oxy}methyl)-3-(2-hydroxyethyl)-1,3-benzoxazol-2(3H)-one

Guidance literature:: With potassium carbonate; In N,N-dimethyl-formamide; at 120 ℃; for 4h; Sealed tube;

Reference yield:

: 63435-16-5
3-hydroxy-4-aminobenzoic acid methyl ester

: 1435516-85-0
6-({[tert-butyl(diphenyl)silyl]oxy}methyl)-3-(2-hydroxyethyl)-1,3-benzoxazol-2(3H)-one

Guidance literature:: Multi-step reaction with 4 steps

1: tetrahydrofuran / 24 h / Reflux

2: lithium aluminium tetrahydride / tetrahydrofuran / 1.58 h / 5 - 20 °C / Inert atmosphere

3: 1H-imidazole / N,N-dimethyl-formamide / 16 h / 0 - 20 °C

4: potassium carbonate / N,N-dimethyl-formamide / 4 h / 120 °C / Sealed tube

With 1H-imidazole; lithium aluminium tetrahydride; potassium carbonate; In tetrahydrofuran; N,N-dimethyl-formamide;

Reference yield:

: 2374-03-0
4-aminosalicylic acid

: 1435516-85-0
6-({[tert-butyl(diphenyl)silyl]oxy}methyl)-3-(2-hydroxyethyl)-1,3-benzoxazol-2(3H)-one

Guidance literature:: Multi-step reaction with 5 steps

1: hydrogenchloride / 48 h / 0 - 20 °C

2: tetrahydrofuran / 24 h / Reflux

3: lithium aluminium tetrahydride / tetrahydrofuran / 1.58 h / 5 - 20 °C / Inert atmosphere

4: 1H-imidazole / N,N-dimethyl-formamide / 16 h / 0 - 20 °C

5: potassium carbonate / N,N-dimethyl-formamide / 4 h / 120 °C / Sealed tube

With 1H-imidazole; hydrogenchloride; lithium aluminium tetrahydride; potassium carbonate; In tetrahydrofuran; N,N-dimethyl-formamide;