Technology Process of 9-(tert-butyl-dimethyl-silanyloxymethyl)-2-[3-(4-methoxy-benzyloxy)-propyl]-3,4a-dimethyl-3-(trimethyl-silanyloxy)-2,3,4,4a,5a,6,7,10a,11,11a-decahydro-1,5,10-trioxa-cyclohepta[b]naphthalene
There total 13 articles about 9-(tert-butyl-dimethyl-silanyloxymethyl)-2-[3-(4-methoxy-benzyloxy)-propyl]-3,4a-dimethyl-3-(trimethyl-silanyloxy)-2,3,4,4a,5a,6,7,10a,11,11a-decahydro-1,5,10-trioxa-cyclohepta[b]naphthalene 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:
-
-
884005-03-2
9-(tert-butyl-dimethyl-silanyloxymethyl)-2-[3-(4-methoxy-benzyloxy)-propyl]-3,4a-dimethyl-3-(trimethyl-silanyloxy)-2,3,4,4a,5a,6,7,10a,11,11a-decahydro-1,5,10-trioxa-cyclohepta[b]naphthalene
- Guidance literature:
-
bis[1,1-di(trifluoromethyl)ethoxy][(2,6-diisopropylphenyl)imino](2-methyl-2-phenylpropylidene)molybdenum;
In
hexane;
at 50 ℃;
for 16h;
DOI:10.1002/chem.200500993
-
-
884005-03-2
9-(tert-butyl-dimethyl-silanyloxymethyl)-2-[3-(4-methoxy-benzyloxy)-propyl]-3,4a-dimethyl-3-(trimethyl-silanyloxy)-2,3,4,4a,5a,6,7,10a,11,11a-decahydro-1,5,10-trioxa-cyclohepta[b]naphthalene
- Guidance literature:
-
Multi-step reaction with 8 steps
1: 2,6-lutidine / CH2Cl2 / -65 °C
2: 2,6-lutidine / 0 °C
3: 88 percent / CuI / diethyl ether / -40 - 20 °C
4: 85 percent / TBAF / tetrahydrofuran / 4 h / 20 °C
5: 95 percent / DCC; DMAP / CH2Cl2 / 4 h / 20 °C
6: 100 percent / i-Pr2NEt; DMAP / CH2Cl2 / 3 h / 20 °C
7: 71 percent / TiCl4; Zn; TMEDA / PbCl2 / tetrahydrofuran / 65 °C
8: 88 percent / Schrock's molybdenum catalyst / hexane / 16 h / 50 °C
With
2,6-dimethylpyridine; dmap; copper(l) iodide; N,N,N,N,-tetramethylethylenediamine; tetrabutyl ammonium fluoride; titanium tetrachloride; N-ethyl-N,N-diisopropylamine; dicyclohexyl-carbodiimide; zinc;
bis[1,1-di(trifluoromethyl)ethoxy][(2,6-diisopropylphenyl)imino](2-methyl-2-phenylpropylidene)molybdenum; lead(II) chloride;
In
tetrahydrofuran; diethyl ether; hexane; dichloromethane;
DOI:10.1002/chem.200500993
-
-
884005-03-2
9-(tert-butyl-dimethyl-silanyloxymethyl)-2-[3-(4-methoxy-benzyloxy)-propyl]-3,4a-dimethyl-3-(trimethyl-silanyloxy)-2,3,4,4a,5a,6,7,10a,11,11a-decahydro-1,5,10-trioxa-cyclohepta[b]naphthalene
- Guidance literature:
-
Multi-step reaction with 9 steps
1: 100 percent / HF*pyridine / tetrahydrofuran / 0 °C
2: 2,6-lutidine / CH2Cl2 / -65 °C
3: 2,6-lutidine / 0 °C
4: 88 percent / CuI / diethyl ether / -40 - 20 °C
5: 85 percent / TBAF / tetrahydrofuran / 4 h / 20 °C
6: 95 percent / DCC; DMAP / CH2Cl2 / 4 h / 20 °C
7: 100 percent / i-Pr2NEt; DMAP / CH2Cl2 / 3 h / 20 °C
8: 71 percent / TiCl4; Zn; TMEDA / PbCl2 / tetrahydrofuran / 65 °C
9: 88 percent / Schrock's molybdenum catalyst / hexane / 16 h / 50 °C
With
2,6-dimethylpyridine; dmap; copper(l) iodide; N,N,N,N,-tetramethylethylenediamine; tetrabutyl ammonium fluoride; titanium tetrachloride; pyridine hydrogenfluoride; N-ethyl-N,N-diisopropylamine; dicyclohexyl-carbodiimide; zinc;
bis[1,1-di(trifluoromethyl)ethoxy][(2,6-diisopropylphenyl)imino](2-methyl-2-phenylpropylidene)molybdenum; lead(II) chloride;
In
tetrahydrofuran; diethyl ether; hexane; dichloromethane;
DOI:10.1002/chem.200500993