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1-[3-(tert-butyl-diphenyl-silanyloxymethyl)-2,3,7,7a,8,9,10,11-octahydro-1H-pyrrolo[2,1-j]quinolin-6-yl]-ethanone

Base Information
  • Chemical Name:1-[3-(tert-butyl-diphenyl-silanyloxymethyl)-2,3,7,7a,8,9,10,11-octahydro-1H-pyrrolo[2,1-j]quinolin-6-yl]-ethanone
  • CAS No.:934296-26-1
  • Molecular Formula:C31H41NO2Si
  • Molecular Weight:487.758
  • Hs Code.:
1-[3-(<i>tert</i>-butyl-diphenyl-silanyloxymethyl)-2,3,7,7a,8,9,10,11-octahydro-1<i>H</i>-pyrrolo[2,1-<i>j</i>]quinolin-6-yl]-ethanone

Synonyms:1-[3-(tert-butyl-diphenyl-silanyloxymethyl)-2,3,7,7a,8,9,10,11-octahydro-1H-pyrrolo[2,1-j]quinolin-6-yl]-ethanone

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Chemical Property of 1-[3-(tert-butyl-diphenyl-silanyloxymethyl)-2,3,7,7a,8,9,10,11-octahydro-1H-pyrrolo[2,1-j]quinolin-6-yl]-ethanone
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Technology Process of 1-[3-(tert-butyl-diphenyl-silanyloxymethyl)-2,3,7,7a,8,9,10,11-octahydro-1H-pyrrolo[2,1-j]quinolin-6-yl]-ethanone

There total 10 articles about 1-[3-(tert-butyl-diphenyl-silanyloxymethyl)-2,3,7,7a,8,9,10,11-octahydro-1H-pyrrolo[2,1-j]quinolin-6-yl]-ethanone 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:
Guidance literature:
2-[4-(tert-butyl-diphenyl-silanyloxy)-3-(3-oxo-but-1-enylamino)-butyl]-cyclohex-1-enecarbaldehyde; With piperdinium acetate; sodium sulfate; In ethyl acetate; for 12h; Heating;
With hydrogen; palladium on activated charcoal; In ethyl acetate; for 4h; under 760 Torr;
Guidance literature:
Multi-step reaction with 10 steps
1.1: aq. K3PO4 / PdCl2(dppf)*CH2Cl2 / tetrahydrofuran / 12 h / Heating
2.1: pyridinium p-toluenesulfonate / methanol / 1 h / Heating
3.1: imidazole / CH2Cl2 / 20 °C
4.1: 12.0 g / DIBAL-H / CH2Cl2 / -78 - 0 °C
5.1: pyridine / 20 °C
6.1: 100 percent / TFA / CH2Cl2 / 1 h / 0 °C
7.1: CH2Cl2 / 40 °C
8.1: K2CO3 / methanol; H2O / 1 h / 20 °C
9.1: N-methylmorpholine-N-oxide; TPAP; 4 Angstroem molecular sieves / CH2Cl2 / 1 h / 20 °C
10.1: piperidinium acetate; Na2SO4 / ethyl acetate / 12 h / Heating
10.2: 50.0 mg / H2 / 10 percent Pd/C / ethyl acetate / 4 h / 760 Torr
With pyridine; 1H-imidazole; potassium phosphate; tetrapropylammonium perruthennate; 4 A molecular sieve; pyridinium p-toluenesulfonate; piperdinium acetate; diisobutylaluminium hydride; potassium carbonate; 4-methylmorpholine N-oxide; sodium sulfate; trifluoroacetic acid; dichloro(1,1'-bis(diphenylphosphanyl)ferrocene)palladium(II)*CH2Cl2; In tetrahydrofuran; methanol; dichloromethane; water; ethyl acetate; 1.1: Suzuki-Miyaura coupling;
Guidance literature:
Multi-step reaction with 4 steps
1.1: CH2Cl2 / 40 °C
2.1: K2CO3 / methanol; H2O / 1 h / 20 °C
3.1: N-methylmorpholine-N-oxide; TPAP; 4 Angstroem molecular sieves / CH2Cl2 / 1 h / 20 °C
4.1: piperidinium acetate; Na2SO4 / ethyl acetate / 12 h / Heating
4.2: 50.0 mg / H2 / 10 percent Pd/C / ethyl acetate / 4 h / 760 Torr
With tetrapropylammonium perruthennate; 4 A molecular sieve; piperdinium acetate; potassium carbonate; 4-methylmorpholine N-oxide; sodium sulfate; In methanol; dichloromethane; water; ethyl acetate;
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