Methyl 2-benzoyl-5-<<(tert-butyl)dimethylsilyl>oxy>biphenyl-3-carboxylate

Base Information

Chemical Name:Methyl 2-benzoyl-5-<<(tert-butyl)dimethylsilyl>oxy>biphenyl-3-carboxylate
CAS No.:133721-60-5
Molecular Formula:C₂₇H₃₀O₄Si
Molecular Weight:446.618
Hs Code.:

Synonyms:Methyl 2-benzoyl-5-<<(tert-butyl)dimethylsilyl>oxy>biphenyl-3-carboxylate

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Business phase:: The product has achieved commercial mass production^*data from LookChem market partment

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Chemical Property of Methyl 2-benzoyl-5-<<(tert-butyl)dimethylsilyl>oxy>biphenyl-3-carboxylate

Chemical Property:

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Technology Process of Methyl 2-benzoyl-5-<<(tert-butyl)dimethylsilyl>oxy>biphenyl-3-carboxylate

There total 6 articles about Methyl 2-benzoyl-5-<<(tert-butyl)dimethylsilyl>oxy>biphenyl-3-carboxylate 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: 98.0%

: 16075-82-4
2,3-Dihydro-2,2-dimethyl-6-phenyl-4H-pyran-4-one

: 69739-34-0
t-butyldimethylsiyl triflate

: 41158-32-1
methyl 4-oxo-4-phenylbut-2-ynoate

: 133721-60-5
Methyl 2-benzoyl-5-<<(tert-butyl)dimethylsilyl>oxy>biphenyl-3-carboxylate

Guidance literature:: With di(tert-butyl)pyridine; In chloroform; 1.) 0 deg C, 2 h, 2.) r.t., 2 h;
DOI:10.1002/hlca.19910740106

Reference yield:

: 40485-33-4
5-Hydroxy-5-methylhex-2-ynophenone

: 133721-60-5
Methyl 2-benzoyl-5-<<(tert-butyl)dimethylsilyl>oxy>biphenyl-3-carboxylate

Guidance literature:: Multi-step reaction with 2 steps

1: 87.3 percent / 33 percent HBr/AcOH / CH₂Cl₂ / 1.) 0 deg C, 30 min, 2.) r.t., 4-10 h

2: 98 percent / di(tert-butyl)pyridine / CHCl₃ / 1.) 0 deg C, 2 h, 2.) r.t., 2 h

With di(tert-butyl)pyridine; hydrogen bromide; acetic acid; In dichloromethane; chloroform;
DOI:10.1002/hlca.19910740106

Reference yield:

: 6919-61-5
N-methoxy-N-methylbenzamide

: 133721-60-5
Methyl 2-benzoyl-5-<<(tert-butyl)dimethylsilyl>oxy>biphenyl-3-carboxylate

Guidance literature:: Multi-step reaction with 3 steps

1: 1.) (i-Pr)MgCl / 1.) THF, r.t., 5 h, 2.) r.t., 12 h

2: 87.3 percent / 33 percent HBr/AcOH / CH₂Cl₂ / 1.) 0 deg C, 30 min, 2.) r.t., 4-10 h

3: 98 percent / di(tert-butyl)pyridine / CHCl₃ / 1.) 0 deg C, 2 h, 2.) r.t., 2 h

With di(tert-butyl)pyridine; hydrogen bromide; isopropylmagnesium chloride; acetic acid; In dichloromethane; chloroform;
DOI:10.1002/hlca.19910740106