(7-bromo-3-phenyl-2,3-dihydro-benzofuran-3-ylmethoxy)-tert-butyl-dimethyl-silane

Base Information

Chemical Name:(7-bromo-3-phenyl-2,3-dihydro-benzofuran-3-ylmethoxy)-tert-butyl-dimethyl-silane
CAS No.:405519-75-7
Molecular Formula:C₂₁H₂₇BrO₂Si
Molecular Weight:419.434
Hs Code.:

(7-bromo-3-phenyl-2,3-dihydro-benzofuran-3-ylmethoxy)-<i>tert</i>-butyl-dimethyl-silane

Synonyms:(7-bromo-3-phenyl-2,3-dihydro-benzofuran-3-ylmethoxy)-tert-butyl-dimethyl-silane

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Chemical Property of (7-bromo-3-phenyl-2,3-dihydro-benzofuran-3-ylmethoxy)-tert-butyl-dimethyl-silane

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Technology Process of (7-bromo-3-phenyl-2,3-dihydro-benzofuran-3-ylmethoxy)-tert-butyl-dimethyl-silane

There total 9 articles about (7-bromo-3-phenyl-2,3-dihydro-benzofuran-3-ylmethoxy)-tert-butyl-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: 95.0%

: 405519-74-6
C₂₁H₂₇BrO₃Si

: 405519-75-7
(7-bromo-3-phenyl-2,3-dihydro-benzofuran-3-ylmethoxy)-tert-butyl-dimethyl-silane

Guidance literature:: With 1,1'-carbonyldiimidazole; In tetrahydrofuran; for 2h; Heating / reflux;

Reference yield: 95.0%

: 2-bromo-6-[2-(tert-butyl-dimethyl-silanyloxy)-1-hydroxymethyl-1-phenyl-ethyl]-phenol

: 405519-75-7
(7-bromo-3-phenyl-2,3-dihydro-benzofuran-3-ylmethoxy)-tert-butyl-dimethyl-silane

Guidance literature:: With 1,1'-carbonyldiimidazole; In tetrahydrofuran; for 2h; Heating;
DOI:10.1002/1521-3773(20011217)40:24<4705::AID-ANIE4705>3.0.CO;2-D

Reference yield:

: 95-56-7
2-hydroxybromobenzene

: 405519-75-7
(7-bromo-3-phenyl-2,3-dihydro-benzofuran-3-ylmethoxy)-tert-butyl-dimethyl-silane

Guidance literature:: Multi-step reaction with 6 steps

1: 42 percent / aq. H₂SO₄ / 45 h / Heating

2: Et₃N / CH₂Cl₂ / 1 h / 0 °C

3: Yb(OTf)3 / tetrahydrofuran; H₂O / 24 h / 25 °C

4: 95 percent / imidazole / dimethylformamide / 6 h / 25 °C

5: 95 percent / LiBH₄ / tetrahydrofuran / 4 h / 25 °C

6: 95 percent / 1,1'-carbonyldiimidazole / tetrahydrofuran / 2 h / Heating

With 1H-imidazole; lithium borohydride; sulfuric acid; triethylamine; 1,1'-carbonyldiimidazole; ytterbium(III) triflate; In tetrahydrofuran; dichloromethane; water; N,N-dimethyl-formamide;
DOI:10.1002/1521-3773(20011217)40:24<4705::AID-ANIE4705>3.0.CO;2-D