1-((1S,3R,4S)-4-Benzyloxy-3-benzyloxymethyl-2-oxo-cyclopentyl)-5-methyl-1H-pyrimidine-2,4-dione

Base Information

Chemical Name:1-((1S,3R,4S)-4-Benzyloxy-3-benzyloxymethyl-2-oxo-cyclopentyl)-5-methyl-1H-pyrimidine-2,4-dione
CAS No.:142217-82-1
Molecular Formula:C₂₅H₂₆N₂O₅
Molecular Weight:434.492
Hs Code.:

Synonyms:

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Chemical Property of 1-((1S,3R,4S)-4-Benzyloxy-3-benzyloxymethyl-2-oxo-cyclopentyl)-5-methyl-1H-pyrimidine-2,4-dione

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Technology Process of 1-((1S,3R,4S)-4-Benzyloxy-3-benzyloxymethyl-2-oxo-cyclopentyl)-5-methyl-1H-pyrimidine-2,4-dione

There total 7 articles about 1-((1S,3R,4S)-4-Benzyloxy-3-benzyloxymethyl-2-oxo-cyclopentyl)-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:

: 3587-60-8
Benzyloxymethyl chloride

: 142217-82-1
1-((1S,3R,4S)-4-Benzyloxy-3-benzyloxymethyl-2-oxo-cyclopentyl)-5-methyl-1H-pyrimidine-2,4-dione

Guidance literature:: Multi-step reaction with 6 steps

1: tetrahydrofuran / -78 - -65 °C

2: 1.) diisopinylcampheylborane (prepared from (+)-α-pinene), 2.) aq. NaOH, H2O2 / 1.) THF, -65 to -78 deg C

3: VO(acac)2, t-BuOOH / CH₂Cl₂

4: NaH, Bu₄NI / dimethylformamide

5: 64 percent / LiH / dimethylformamide / 140 °C

6: DMSO, DCC, CH₃PO₃H₂

With tert.-butylhydroperoxide; sodium hydroxide; bis(acetylacetonate)oxovanadium; (-)-diisopinocampheylborane; methylphosphonic acid; dihydrogen peroxide; tetra-(n-butyl)ammonium iodide; lithium hydride; sodium hydride; dimethyl sulfoxide; dicyclohexyl-carbodiimide; In tetrahydrofuran; dichloromethane; N,N-dimethyl-formamide;
DOI:10.1016/S0960-894X(96)00594-X

Reference yield:

: 39939-07-6
5-(benzyloxymethyl)cyclopentadiene

: 142217-82-1
1-((1S,3R,4S)-4-Benzyloxy-3-benzyloxymethyl-2-oxo-cyclopentyl)-5-methyl-1H-pyrimidine-2,4-dione

Guidance literature:: Multi-step reaction with 5 steps

1: 1.) diisopinylcampheylborane (prepared from (+)-α-pinene), 2.) aq. NaOH, H2O2 / 1.) THF, -65 to -78 deg C

2: VO(acac)2, t-BuOOH / CH₂Cl₂

3: NaH, Bu₄NI / dimethylformamide

4: 64 percent / LiH / dimethylformamide / 140 °C

5: DMSO, DCC, CH₃PO₃H₂

With tert.-butylhydroperoxide; sodium hydroxide; bis(acetylacetonate)oxovanadium; (-)-diisopinocampheylborane; methylphosphonic acid; dihydrogen peroxide; tetra-(n-butyl)ammonium iodide; lithium hydride; sodium hydride; dimethyl sulfoxide; dicyclohexyl-carbodiimide; In dichloromethane; N,N-dimethyl-formamide;
DOI:10.1016/S0960-894X(96)00594-X

Reference yield:

: 110567-22-1
(2R,3S)-benzyloxy-2-benzyloxymethyl-6-oxabicyclo<3.1.0>hexane

: 142217-82-1
1-((1S,3R,4S)-4-Benzyloxy-3-benzyloxymethyl-2-oxo-cyclopentyl)-5-methyl-1H-pyrimidine-2,4-dione

Guidance literature:: Multi-step reaction with 2 steps

1: 64 percent / LiH / dimethylformamide / 140 °C

2: DMSO, DCC, CH₃PO₃H₂

With methylphosphonic acid; lithium hydride; dimethyl sulfoxide; dicyclohexyl-carbodiimide; In N,N-dimethyl-formamide;
DOI:10.1016/S0960-894X(96)00594-X