6-(tert-Butyl-diphenyl-silanyloxy)-4-methyl-1,4-dihydro-naphtho[2,1-d][1,3]oxazin-3-one

Base Information

Chemical Name:6-(tert-Butyl-diphenyl-silanyloxy)-4-methyl-1,4-dihydro-naphtho[2,1-d][1,3]oxazin-3-one
CAS No.:157528-29-5
Molecular Formula:C₂₉H₂₉NO₃Si
Molecular Weight:467.64
Hs Code.:

Synonyms:6-(tert-Butyl-diphenyl-silanyloxy)-4-methyl-1,4-dihydro-naphtho[2,1-d][1,3]oxazin-3-one

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Chemical Property of 6-(tert-Butyl-diphenyl-silanyloxy)-4-methyl-1,4-dihydro-naphtho[2,1-d][1,3]oxazin-3-one

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Technology Process of 6-(tert-Butyl-diphenyl-silanyloxy)-4-methyl-1,4-dihydro-naphtho[2,1-d][1,3]oxazin-3-one

There total 9 articles about 6-(tert-Butyl-diphenyl-silanyloxy)-4-methyl-1,4-dihydro-naphtho[2,1-d][1,3]oxazin-3-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: 90.0%

: 157528-28-4
[4-(tert-Butyl-diphenyl-silanyloxy)-1-(tert-butyl-diphenyl-silanyloxymethyl)-naphthalen-2-yl]-methyl-carbamic acid tert-butyl ester

: 157528-29-5
6-(tert-Butyl-diphenyl-silanyloxy)-4-methyl-1,4-dihydro-naphtho[2,1-d][1,3]oxazin-3-one

Guidance literature:: 9-BBN triflate; In dichloromethane; at -78 ℃; for 0.25h;
DOI:10.1021/jo00096a043

Reference yield:

: 122745-37-3
2-((tert-Butyloxycarbonyl)amino)-4-(benzyloxy)-1-bromonaphthalene

: 157528-29-5
6-(tert-Butyl-diphenyl-silanyloxy)-4-methyl-1,4-dihydro-naphtho[2,1-d][1,3]oxazin-3-one

Guidance literature:: Multi-step reaction with 6 steps

1: 94 percent / NaH / dimethylformamide / 1.) 25 deg C, 30 min, 2.) 25 deg C, 2 h

2: 1.) n-BuLi, 2.) H₂ / 2.) 10percent Pd-C

3: 91 percent / DMAP / dioxane / 1 h / 100 °C

4: 76 percent / NaBH₄ / ethanol / 0.5 h / 25 °C

5: 43 percent / imidazole / dimethylformamide / 1 h / 100 °C

6: 90 percent / 9-BBN-OTf / CH₂Cl₂ / 0.25 h / -78 °C

With 1H-imidazole; dmap; sodium tetrahydroborate; n-butyllithium; hydrogen; sodium hydride; palladium on activated charcoal; 9-BBN triflate; In 1,4-dioxane; ethanol; dichloromethane; N,N-dimethyl-formamide;
DOI:10.1021/jo00096a043

Reference yield:

: 122745-36-2
N-(tert-butyloxycarbonyl)-4-(benzyloxy)-2-naphthylamine

: 157528-29-5
6-(tert-Butyl-diphenyl-silanyloxy)-4-methyl-1,4-dihydro-naphtho[2,1-d][1,3]oxazin-3-one

Guidance literature:: Multi-step reaction with 7 steps

1: 97 percent / conc. H₂SO₄, NBS / tetrahydrofuran / 1.) -78 deg C, 5 min, 2.) -78 deg C, 5 h

2: 94 percent / NaH / dimethylformamide / 1.) 25 deg C, 30 min, 2.) 25 deg C, 2 h

3: 1.) n-BuLi, 2.) H₂ / 2.) 10percent Pd-C

4: 91 percent / DMAP / dioxane / 1 h / 100 °C

5: 76 percent / NaBH₄ / ethanol / 0.5 h / 25 °C

6: 43 percent / imidazole / dimethylformamide / 1 h / 100 °C

7: 90 percent / 9-BBN-OTf / CH₂Cl₂ / 0.25 h / -78 °C

With 1H-imidazole; dmap; sodium tetrahydroborate; N-Bromosuccinimide; n-butyllithium; sulfuric acid; hydrogen; sodium hydride; palladium on activated charcoal; 9-BBN triflate; In tetrahydrofuran; 1,4-dioxane; ethanol; dichloromethane; N,N-dimethyl-formamide;
DOI:10.1021/jo00096a043