3-benzoyl-1-[6-(tert-butyl-dimethyl-silanyloxy)-spiro[4.4]non-2-yl]-5-methyl-1H-pyrimidine-2,4-dione

Base Information

Chemical Name:3-benzoyl-1-[6-(tert-butyl-dimethyl-silanyloxy)-spiro[4.4]non-2-yl]-5-methyl-1H-pyrimidine-2,4-dione
CAS No.:511549-86-3
Molecular Formula:C₂₇H₃₈N₂O₄Si
Molecular Weight:482.695
Hs Code.:

3-benzoyl-1-[6-(<i>tert</i>-butyl-dimethyl-silanyloxy)-spiro[4.4]non-2-yl]-5-methyl-1<i>H</i>-pyrimidine-2,4-dione

Synonyms:3-benzoyl-1-[6-(tert-butyl-dimethyl-silanyloxy)-spiro[4.4]non-2-yl]-5-methyl-1H-pyrimidine-2,4-dione

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Chemical Property of 3-benzoyl-1-[6-(tert-butyl-dimethyl-silanyloxy)-spiro[4.4]non-2-yl]-5-methyl-1H-pyrimidine-2,4-dione

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Technology Process of 3-benzoyl-1-[6-(tert-butyl-dimethyl-silanyloxy)-spiro[4.4]non-2-yl]-5-methyl-1H-pyrimidine-2,4-dione

There total 8 articles about 3-benzoyl-1-[6-(tert-butyl-dimethyl-silanyloxy)-spiro[4.4]non-2-yl]-5-methyl-1H-pyrimidine-2,4-dione 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: 30.0%

: 4330-20-5
N-3-benzoylthymine

: 511549-83-0
(2R,5R,6R)-6-(tert-Butyl-dimethyl-silanyloxy)-spiro[4.4]nonan-2-ol

: 511549-86-3
3-benzoyl-1-[6-(tert-butyl-dimethyl-silanyloxy)-spiro[4.4]non-2-yl]-5-methyl-1H-pyrimidine-2,4-dione

Guidance literature:: With di-isopropyl azodicarboxylate; triphenylphosphine;
DOI:10.1021/ol0340033

Reference yield:

: 511549-78-3
tert-Butyl-dimethyl-((1R,5S)-spiro[4.4]non-6-en-1-yloxy)-silane

: 511549-86-3
3-benzoyl-1-[6-(tert-butyl-dimethyl-silanyloxy)-spiro[4.4]non-2-yl]-5-methyl-1H-pyrimidine-2,4-dione

Guidance literature:: Multi-step reaction with 4 steps

1: 53 percent / CrO₃; 3,5-DMP

2: NaBH₄; CeCl₃

3: 72 percent / H₂ / Pd/C

4: 30 percent / DIAD; Ph₃P

With chromium(VI) oxide; sodium tetrahydroborate; cerium(III) chloride; di-isopropyl azodicarboxylate; hydrogen; triphenylphosphine; 3,5-Dimethylphenol; palladium on activated charcoal; 4: Mitsunobu reaction;

Reference yield:

: 511549-79-4
(5S,6R)-6-(tert-Butyl-dimethyl-silanyloxy)-spiro[4.4]non-3-en-2-one

: 511549-86-3
3-benzoyl-1-[6-(tert-butyl-dimethyl-silanyloxy)-spiro[4.4]non-2-yl]-5-methyl-1H-pyrimidine-2,4-dione

Guidance literature:: Multi-step reaction with 3 steps

1: NaBH₄; CeCl₃

2: 72 percent / H₂ / Pd/C

3: 30 percent / DIAD; Ph₃P

With sodium tetrahydroborate; cerium(III) chloride; di-isopropyl azodicarboxylate; hydrogen; triphenylphosphine; palladium on activated charcoal; 3: Mitsunobu reaction;