2,3,5-tri-O-benzyl-N,N',N'-tris-t-butyloxycarbonyl-4-O-trimethylsilyl-D-arabinonohydrazide

Base Information

Chemical Name:2,3,5-tri-O-benzyl-N,N',N'-tris-t-butyloxycarbonyl-4-O-trimethylsilyl-D-arabinonohydrazide
CAS No.:137272-02-7
Molecular Formula:C₄₄H₆₂N₂O₁₁Si
Molecular Weight:823.069
Hs Code.:

Synonyms:2,3,5-tri-O-benzyl-N,N',N'-tris-t-butyloxycarbonyl-4-O-trimethylsilyl-D-arabinonohydrazide

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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 2,3,5-tri-O-benzyl-N,N',N'-tris-t-butyloxycarbonyl-4-O-trimethylsilyl-D-arabinonohydrazide

Chemical Property:

Purity/Quality:: 98% ^*data from raw suppliers

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Technology Process of 2,3,5-tri-O-benzyl-N,N',N'-tris-t-butyloxycarbonyl-4-O-trimethylsilyl-D-arabinonohydrazide

There total 4 articles about 2,3,5-tri-O-benzyl-N,N',N'-tris-t-butyloxycarbonyl-4-O-trimethylsilyl-D-arabinonohydrazide 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: 80.0%

: 24424-99-5
di-tert-butyl dicarbonate

: 137272-00-5
2,3,5-tri-O-benzyl-N'-t-butyloxycarbonyl-4-O-trimethylsilyl-D-arabinonohydrazide

: 137272-02-7
2,3,5-tri-O-benzyl-N,N',N'-tris-t-butyloxycarbonyl-4-O-trimethylsilyl-D-arabinonohydrazide

Guidance literature:: With 4-pyrrolidin-1-ylpyridine; triethylamine; In dichloromethane; for 20h; Ambient temperature;
DOI:10.1016/S0040-4020(01)86557-1

Reference yield:

: 14233-64-8
tri-O-benzyl-D-arabinolactone

: 137272-02-7
2,3,5-tri-O-benzyl-N,N',N'-tris-t-butyloxycarbonyl-4-O-trimethylsilyl-D-arabinonohydrazide

Guidance literature:: Multi-step reaction with 4 steps

1: 90 percent / NH₂NH₂*H₂O / methanol; CH₂Cl₂ / 2 h / Ambient temperature

2: 100 percent / CH₂Cl₂ / 60 h / Ambient temperature

3: 66 percent / Et₃N / CH₂Cl₂ / 24 h / Ambient temperature

4: 80 percent / Et₃N, 4-pyrrolidinopyridine / CH₂Cl₂ / 20 h / Ambient temperature

With 4-pyrrolidin-1-ylpyridine; hydrazine hydrate; triethylamine; In methanol; dichloromethane;
DOI:10.1016/S0040-4020(01)86557-1

Reference yield:

: 137271-98-8
2,3,5-tri-O-benzyl-D-arabinonohydrazide

: 137272-02-7
2,3,5-tri-O-benzyl-N,N',N'-tris-t-butyloxycarbonyl-4-O-trimethylsilyl-D-arabinonohydrazide

Guidance literature:: Multi-step reaction with 3 steps

1: 100 percent / CH₂Cl₂ / 60 h / Ambient temperature

2: 66 percent / Et₃N / CH₂Cl₂ / 24 h / Ambient temperature

3: 80 percent / Et₃N, 4-pyrrolidinopyridine / CH₂Cl₂ / 20 h / Ambient temperature

With 4-pyrrolidin-1-ylpyridine; triethylamine; In dichloromethane;
DOI:10.1016/S0040-4020(01)86557-1