tert-butyl-[2-(4-methoxy-phenyl)-dihydro-furo[2,3-d][1,3]dioxol-3a-ylmethoxy]-dimethyl-silane

Base Information

• Chemical Name: tert-butyl-[2-(4-methoxy-phenyl)-dihydro-furo[2,3-d][1,3]dioxol-3a-ylmethoxy]-dimethyl-silane
• CAS No.: 615265-12-8
• Molecular Formula: C₁₉H₃₀O₅Si
• Molecular Weight: 366.53

Synonyms:tert-butyl-[2-(4-methoxy-phenyl)-dihydro-furo[2,3-d][1,3]dioxol-3a-ylmethoxy]-dimethyl-silane

Chemical Property of tert-butyl-[2-(4-methoxy-phenyl)-dihydro-furo[2,3-d][1,3]dioxol-3a-ylmethoxy]-dimethyl-silane

Chemical Property:

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Technology Process of tert-butyl-[2-(4-methoxy-phenyl)-dihydro-furo[2,3-d][1,3]dioxol-3a-ylmethoxy]-dimethyl-silane

There total 3 articles about tert-butyl-[2-(4-methoxy-phenyl)-dihydro-furo[2,3-d][1,3]dioxol-3a-ylmethoxy]-dimethyl-silane 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: 72.0%

imidazole-1-carbothioic acid O-[3a-(tert-butyl-dimethyl-silanyloxymethyl)-2-(4-methoxy-phenyl)-tetrahydro-furo[2,3-d][1,3]dioxol-6-yl] ester → tert-butyl-[2-(4-methoxy-phenyl)-dihydro-furo[2,3-d][1,3]dioxol-3a-ylmethoxy]-dimethyl-silane (615265-12-8)

Guidance literature:

With tri-n-butylstannate; In toluene; Heating;

DOI:10.1016/S0040-4039(03)01682-4

Reference yield:

tert-butyldimethylsilyl chloride (18162-48-6) → tert-butyl-[2-(4-methoxy-phenyl)-dihydro-furo[2,3-d][1,3]dioxol-3a-ylmethoxy]-dimethyl-silane (615265-12-8)

Guidance literature:

Multi-step reaction with 3 steps

1: 72 percent / pyridine

2: 92 percent / DMAP / tetrahydrofuran

3: 72 percent / tri-n-butylstannate / toluene / Heating

With dmap; tri-n-butylstannate; In tetrahydrofuran; pyridine; toluene;

DOI:10.1016/S0040-4039(03)01682-4

Reference yield:

(3aS,6R,6aS)-3a-Hydroxymethyl-2-(4-methoxy-phenyl)-tetrahydro-furo[2,3-d][1,3]dioxol-6-ol (204650-72-6) → tert-butyl-[2-(4-methoxy-phenyl)-dihydro-furo[2,3-d][1,3]dioxol-3a-ylmethoxy]-dimethyl-silane (615265-12-8)

Guidance literature:

Multi-step reaction with 3 steps

1: 72 percent / pyridine

2: 92 percent / DMAP / tetrahydrofuran

3: 72 percent / tri-n-butylstannate / toluene / Heating

With dmap; tri-n-butylstannate; In tetrahydrofuran; pyridine; toluene;

DOI:10.1016/S0040-4039(03)01682-4

upstream raw materials:

tert-butyldimethylsilyl chloride

(3aS,6R,6aS)-3a-Hydroxymethyl-2-(4-methoxy-phenyl)-tetrahydro-furo[2,3-d][1,3]dioxol-6-ol

Downstream raw materials:

[(3aS,6aS)-2-(4-Methoxy-phenyl)-dihydro-furo[2,3-d][1,3]dioxol-3a-yl]-methanol

3-Oxo-decanoic acid (3aS,6aS)-2-(4-methoxy-phenyl)-dihydro-furo[2,3-d][1,3]dioxol-3a-ylmethyl ester

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