4-benzyloxy-1-[5-[bis-(4-methoxy-phenyl)-phenyl-methoxymethyl]-4-(tert-butyl-dimethyl-silanyloxy)-tetrahydro-furan-2-yl]-5-methyl-1H-pyrimidin-2-one

Base Information

Chemical Name:4-benzyloxy-1-[5-[bis-(4-methoxy-phenyl)-phenyl-methoxymethyl]-4-(tert-butyl-dimethyl-silanyloxy)-tetrahydro-furan-2-yl]-5-methyl-1H-pyrimidin-2-one
CAS No.:291753-09-8
Molecular Formula:C₄₄H₅₂N₂O₇Si
Molecular Weight:748.992
Hs Code.:

4-benzyloxy-1-[5-[bis-(4-methoxy-phenyl)-phenyl-methoxymethyl]-4-(<i>tert</i>-butyl-dimethyl-silanyloxy)-tetrahydro-furan-2-yl]-5-methyl-1<i>H</i>-pyrimidin-2-one

Synonyms:4-benzyloxy-1-[5-[bis-(4-methoxy-phenyl)-phenyl-methoxymethyl]-4-(tert-butyl-dimethyl-silanyloxy)-tetrahydro-furan-2-yl]-5-methyl-1H-pyrimidin-2-one

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Chemical Property of 4-benzyloxy-1-[5-[bis-(4-methoxy-phenyl)-phenyl-methoxymethyl]-4-(tert-butyl-dimethyl-silanyloxy)-tetrahydro-furan-2-yl]-5-methyl-1H-pyrimidin-2-one

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Technology Process of 4-benzyloxy-1-[5-[bis-(4-methoxy-phenyl)-phenyl-methoxymethyl]-4-(tert-butyl-dimethyl-silanyloxy)-tetrahydro-furan-2-yl]-5-methyl-1H-pyrimidin-2-one

There total 1 articles about 4-benzyloxy-1-[5-[bis-(4-methoxy-phenyl)-phenyl-methoxymethyl]-4-(tert-butyl-dimethyl-silanyloxy)-tetrahydro-furan-2-yl]-5-methyl-1H-pyrimidin-2-one 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:

: Toluene-4-sulfonic acid 1-[(2R,4S,5R)-5-[bis-(4-methoxy-phenyl)-phenyl-methoxymethyl]-4-(tert-butyl-dimethyl-silanyloxy)-tetrahydro-furan-2-yl]-5-methyl-2-oxo-1,2-dihydro-pyrimidin-4-yl ester

: 100-51-6,185532-71-2
benzyl alcohol

: 291753-09-8
4-benzyloxy-1-[5-[bis-(4-methoxy-phenyl)-phenyl-methoxymethyl]-4-(tert-butyl-dimethyl-silanyloxy)-tetrahydro-furan-2-yl]-5-methyl-1H-pyrimidin-2-one

Guidance literature:: With 1,8-diazabicyclo[5.4.0]undec-7-ene;
DOI:10.1016/S0040-4039(00)00662-6

Reference yield: 87.0%

: 291753-09-8
4-benzyloxy-1-[5-[bis-(4-methoxy-phenyl)-phenyl-methoxymethyl]-4-(tert-butyl-dimethyl-silanyloxy)-tetrahydro-furan-2-yl]-5-methyl-1H-pyrimidin-2-one

: 291753-10-1
4-benzyloxy-1-[4-(tert-butyl-dimethyl-silanyloxy)-5-hydroxymethyl-tetrahydro-furan-2-yl]-5-methyl-1H-pyrimidin-2-one

Guidance literature:: With dichloro-acetic acid; In dichloromethane;
DOI:10.1016/S0040-4039(00)00662-6

Reference yield:

: 291753-09-8
4-benzyloxy-1-[5-[bis-(4-methoxy-phenyl)-phenyl-methoxymethyl]-4-(tert-butyl-dimethyl-silanyloxy)-tetrahydro-furan-2-yl]-5-methyl-1H-pyrimidin-2-one

: 291753-12-3
1-[5-(benzyloxyamino-methyl)-4-(tert-butyl-dimethyl-silanyloxy)-tetrahydro-furan-2-yl]-5-methyl-1H-pyrimidine-2,4-dione

Guidance literature:: Multi-step reaction with 3 steps

1: 87 percent / HCCl₂COOH / CH₂Cl₂

2: 87 percent / Ph₃P; DBAD / tetrahydrofuran

3: 99 percent / TFA / CH₂Cl₂

With dichloro-acetic acid; dibenzyl azodicarboxylate; triphenylphosphine; trifluoroacetic acid; In tetrahydrofuran; dichloromethane; 1: ether cleavage / 2: Mitsunobu reaction / 3: ether cleavage; carbamate cleavage;
DOI:10.1016/S0040-4039(00)00662-6