4-benzyloxy-6-butyl-5-{4-(tert-butyldimethylsilyloxy-3,5-dipropylbenzyl)}-2-methylpyrimidine

Base Information

Chemical Name:4-benzyloxy-6-butyl-5-{4-(tert-butyldimethylsilyloxy-3,5-dipropylbenzyl)}-2-methylpyrimidine
CAS No.:1256780-35-4
Molecular Formula:C₃₅H₅₂N₂O₂Si
Molecular Weight:560.896
Hs Code.:

Synonyms:4-benzyloxy-6-butyl-5-{4-(tert-butyldimethylsilyloxy-3,5-dipropylbenzyl)}-2-methylpyrimidine

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Chemical Property of 4-benzyloxy-6-butyl-5-{4-(tert-butyldimethylsilyloxy-3,5-dipropylbenzyl)}-2-methylpyrimidine

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Technology Process of 4-benzyloxy-6-butyl-5-{4-(tert-butyldimethylsilyloxy-3,5-dipropylbenzyl)}-2-methylpyrimidine

There total 4 articles about 4-benzyloxy-6-butyl-5-{4-(tert-butyldimethylsilyloxy-3,5-dipropylbenzyl)}-2-methylpyrimidine 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: 60.3%

: 1256780-33-2
6-butyl-5-{4-(tert-butyldimethylsilyloxy)-3,5-dipropylbenzyl}-2-methylpyrimidin-4(3H)-one

: 100-39-0
benzyl bromide

: 1256780-35-4
4-benzyloxy-6-butyl-5-{4-(tert-butyldimethylsilyloxy-3,5-dipropylbenzyl)}-2-methylpyrimidine

: 1256780-34-3
3-benzyl-6-butyl-5-[4-(tert-butyldimethylsilyloxy-3,5-dipropylbenzyl)]-2-methylpyrimidin-4(3H)-one

Guidance literature:: With sodium hydride; In N,N-dimethyl-formamide; mineral oil; at 75 ℃; for 15h; cooling with ice;

Reference yield:

: 137421-55-7
t-butyl-dimethylsilyloxy-2,6-dipropyl-4-hydroxymethyl benzene

: 1256780-35-4
4-benzyloxy-6-butyl-5-{4-(tert-butyldimethylsilyloxy-3,5-dipropylbenzyl)}-2-methylpyrimidine

: 1256780-34-3
3-benzyl-6-butyl-5-[4-(tert-butyldimethylsilyloxy-3,5-dipropylbenzyl)]-2-methylpyrimidin-4(3H)-one

Guidance literature:: Multi-step reaction with 4 steps

1.1: phosphorus tribromide / toluene / 1 h / 20 °C / cooling with ice

2.1: sodium hydride / N,N-dimethyl-formamide; mineral oil / 0.5 h / 0 °C

2.2: 18 h / 20 °C

3.1: sodium methylate / methanol / 6 h / Reflux

4.1: sodium hydride / N,N-dimethyl-formamide; mineral oil / 15 h / 75 °C / cooling with ice

With sodium methylate; phosphorus tribromide; sodium hydride; In methanol; N,N-dimethyl-formamide; toluene; mineral oil;

Reference yield:

: 1256779-86-8
methyl 2-{4-(tert-butyldimethylsilyloxy)-3,5-dipropylbenzyl}-3-oxo heptanate

: 1256780-35-4
4-benzyloxy-6-butyl-5-{4-(tert-butyldimethylsilyloxy-3,5-dipropylbenzyl)}-2-methylpyrimidine

: 1256780-34-3
3-benzyl-6-butyl-5-[4-(tert-butyldimethylsilyloxy-3,5-dipropylbenzyl)]-2-methylpyrimidin-4(3H)-one

Guidance literature:: Multi-step reaction with 2 steps

1: sodium methylate / methanol / 6 h / Reflux

2: sodium hydride / N,N-dimethyl-formamide; mineral oil / 15 h / 75 °C / cooling with ice

With sodium methylate; sodium hydride; In methanol; N,N-dimethyl-formamide; mineral oil;