1D-1-O-(tert-butyldiphenylsilyl)-4-O-(trimethylacetyl)-2,3-O-(D-1',7',7'-trimethyl<2.2.1>bicyclohept-2'-ylidene)-myo-inositol

Base Information

Chemical Name:1D-1-O-(tert-butyldiphenylsilyl)-4-O-(trimethylacetyl)-2,3-O-(D-1',7',7'-trimethyl<2.2.1>bicyclohept-2'-ylidene)-myo-inositol
CAS No.:142563-76-6
Molecular Formula:C₃₇H₅₂O₇Si
Molecular Weight:636.901
Hs Code.:

Synonyms:1D-1-O-(tert-butyldiphenylsilyl)-4-O-(trimethylacetyl)-2,3-O-(D-1',7',7'-trimethyl<2.2.1>bicyclohept-2'-ylidene)-myo-inositol

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Chemical Property of 1D-1-O-(tert-butyldiphenylsilyl)-4-O-(trimethylacetyl)-2,3-O-(D-1',7',7'-trimethyl<2.2.1>bicyclohept-2'-ylidene)-myo-inositol

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Technology Process of 1D-1-O-(tert-butyldiphenylsilyl)-4-O-(trimethylacetyl)-2,3-O-(D-1',7',7'-trimethyl<2.2.1>bicyclohept-2'-ylidene)-myo-inositol

There total 6 articles about 1D-1-O-(tert-butyldiphenylsilyl)-4-O-(trimethylacetyl)-2,3-O-(D-1',7',7'-trimethyl<2.2.1>bicyclohept-2'-ylidene)-myo-inositol 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:

: 142534-51-8,142630-97-5
C₄₂H₆₀O₉Si₂

: 142563-76-6
1D-1-O-(tert-butyldiphenylsilyl)-4-O-(trimethylacetyl)-2,3-O-(D-1',7',7'-trimethyl<2.2.1>bicyclohept-2'-ylidene)-myo-inositol

Guidance literature:: Multi-step reaction with 4 steps

1: tetra-n-butylammonium fluoride / tetrahydrofuran / 1 h

2: methylamine / toluene / 48 h / Ambient temperature

3: 88 percent / imidazole, pyridine / 24 h / -10 °C

4: pyridine / 3 h / -10 °C

With pyridine; 1H-imidazole; tetrabutyl ammonium fluoride; methylamine; In tetrahydrofuran; toluene;
DOI:10.1021/ja00042a011

Reference yield:

: C₃₀H₃₄O₈

: 142563-76-6
1D-1-O-(tert-butyldiphenylsilyl)-4-O-(trimethylacetyl)-2,3-O-(D-1',7',7'-trimethyl<2.2.1>bicyclohept-2'-ylidene)-myo-inositol

Guidance literature:: Multi-step reaction with 3 steps

1: methylamine / toluene / 48 h / Ambient temperature

2: 88 percent / imidazole, pyridine / 24 h / -10 °C

3: pyridine / 3 h / -10 °C

With pyridine; 1H-imidazole; methylamine; In toluene;
DOI:10.1021/ja00042a011