2-Oxo-3-benzyloxycarbonyl-3',5'-di-O-benzoyl-α-D-ribofurano<1',2':4,5>-oxazolidin

Base Information

Chemical Name:2-Oxo-3-benzyloxycarbonyl-3',5'-di-O-benzoyl-α-D-ribofurano<1',2':4,5>-oxazolidin
CAS No.:81026-82-6
Molecular Formula:C₂₈H₂₃NO₉
Molecular Weight:517.492
Hs Code.:

Synonyms:2-Oxo-3-benzyloxycarbonyl-3',5'-di-O-benzoyl-α-D-ribofurano<1',2':4,5>-oxazolidin

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Chemical Property of 2-Oxo-3-benzyloxycarbonyl-3',5'-di-O-benzoyl-α-D-ribofurano<1',2':4,5>-oxazolidin

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Technology Process of 2-Oxo-3-benzyloxycarbonyl-3',5'-di-O-benzoyl-α-D-ribofurano<1',2':4,5>-oxazolidin

There total 3 articles about 2-Oxo-3-benzyloxycarbonyl-3',5'-di-O-benzoyl-α-D-ribofurano<1',2':4,5>-oxazolidin 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: 96.4%

: 613-90-1
benzoyl cyanide

: 81026-84-8
(3aS,5R,6R,6aR)-6-Hydroxy-5-hydroxymethyl-2-oxo-tetrahydro-furo[2,3-d]oxazole-3-carboxylic acid benzyl ester

: 81026-82-6
2-Oxo-3-benzyloxycarbonyl-3',5'-di-O-benzoyl-α-D-ribofurano<1',2':4,5>-oxazolidin

Guidance literature:: With triethylamine; In acetonitrile; for 24h;

Reference yield:

: 501-53-1,94274-21-2
benzyl chloroformate

: 81026-82-6
2-Oxo-3-benzyloxycarbonyl-3',5'-di-O-benzoyl-α-D-ribofurano<1',2':4,5>-oxazolidin

Guidance literature:: Multi-step reaction with 2 steps

1: 36 percent / acetone; H₂O / Ambient temperature

2: 96.4 percent / Et₃N / acetonitrile / 24 h

With triethylamine; In water; acetone; acetonitrile;

Reference yield:

: 27963-97-9
2-amino-(1,2-dideoxy-α-D-ribofurano)<1,2-d>-2-oxazoline

: 81026-82-6
2-Oxo-3-benzyloxycarbonyl-3',5'-di-O-benzoyl-α-D-ribofurano<1',2':4,5>-oxazolidin

Guidance literature:: Multi-step reaction with 2 steps

1: 36 percent / acetone; H₂O / Ambient temperature

2: 96.4 percent / Et₃N / acetonitrile / 24 h

With triethylamine; In water; acetone; acetonitrile;