Technology Process of tert-Butyl-{(1S,2R,4aR,5R)-2,5-dimethyl-5-phenylsulfanylmethyl-1-[2-(tetrahydro-pyran-2-yloxy)-ethyl]-1,2,3,4,4a,5,6,7-octahydro-naphthalen-1-ylmethoxy}-dimethyl-silane
There total 8 articles about tert-Butyl-{(1S,2R,4aR,5R)-2,5-dimethyl-5-phenylsulfanylmethyl-1-[2-(tetrahydro-pyran-2-yloxy)-ethyl]-1,2,3,4,4a,5,6,7-octahydro-naphthalen-1-ylmethoxy}-dimethyl-silane which
guide to synthetic route it.
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synthetic route:
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535933-03-0
tert-Butyl-{(1S,2R,4aR,5R)-2,5-dimethyl-5-phenylsulfanylmethyl-1-[2-(tetrahydro-pyran-2-yloxy)-ethyl]-1,2,3,4,4a,5,6,7-octahydro-naphthalen-1-ylmethoxy}-dimethyl-silane
- Guidance literature:
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With
pyridine; thionyl chloride;
at 0 ℃;
for 1h;
DOI:10.1021/jo020743y
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535933-03-0
tert-Butyl-{(1S,2R,4aR,5R)-2,5-dimethyl-5-phenylsulfanylmethyl-1-[2-(tetrahydro-pyran-2-yloxy)-ethyl]-1,2,3,4,4a,5,6,7-octahydro-naphthalen-1-ylmethoxy}-dimethyl-silane
- Guidance literature:
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Multi-step reaction with 6 steps
1.1: 86 percent / Bu3P; pyridine / 2 h / 60 °C
2.1: BuLi; diisopropylamine / tetrahydrofuran; hexane / 0.5 h / 0 °C
2.2: 94 percent / HMPA / tetrahydrofuran; hexane / 3 h / 0 °C
3.1: DIBAL-H / hexane; toluene / 4 h / -78 °C
4.1: 209 mg / LiBH4 / tetrahydrofuran / 1 h / 40 °C
5.1: 100 percent / imidazole / dimethylformamide / 4 h / 20 °C
6.1: 93 percent / SOCl2; pyridine / 1 h / 0 °C
With
pyridine; 1H-imidazole; lithium borohydride; n-butyllithium; thionyl chloride; tributylphosphine; diisobutylaluminium hydride; diisopropylamine;
In
tetrahydrofuran; hexane; N,N-dimethyl-formamide; toluene;
DOI:10.1021/jo020743y
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331661-83-7
(2aS,3R,6R,8aR,8bS)-6-Hydroxymethyl-3,6-dimethyl-2a,3,4,6,7,8,8a,8b-octahydro-naphtho[1,8-bc]furan-2-one
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535933-03-0
tert-Butyl-{(1S,2R,4aR,5R)-2,5-dimethyl-5-phenylsulfanylmethyl-1-[2-(tetrahydro-pyran-2-yloxy)-ethyl]-1,2,3,4,4a,5,6,7-octahydro-naphthalen-1-ylmethoxy}-dimethyl-silane
- Guidance literature:
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Multi-step reaction with 7 steps
1.1: 89 percent / H2; PtO2 / acetic acid / 72 h / 20 °C / 3344 Torr
2.1: 86 percent / Bu3P; pyridine / 2 h / 60 °C
3.1: BuLi; diisopropylamine / tetrahydrofuran; hexane / 0.5 h / 0 °C
3.2: 94 percent / HMPA / tetrahydrofuran; hexane / 3 h / 0 °C
4.1: DIBAL-H / hexane; toluene / 4 h / -78 °C
5.1: 209 mg / LiBH4 / tetrahydrofuran / 1 h / 40 °C
6.1: 100 percent / imidazole / dimethylformamide / 4 h / 20 °C
7.1: 93 percent / SOCl2; pyridine / 1 h / 0 °C
With
pyridine; 1H-imidazole; platinum(IV) oxide; lithium borohydride; n-butyllithium; thionyl chloride; tributylphosphine; hydrogen; diisobutylaluminium hydride; diisopropylamine;
In
tetrahydrofuran; hexane; acetic acid; N,N-dimethyl-formamide; toluene;
DOI:10.1021/jo020743y