3-O-benzoyl-6-bromo-6-deoxy-1,2-O-isopropylidene-5-O-p-nitrobenzoyl-β-L-idofuranose

Base Information

Chemical Name:3-O-benzoyl-6-bromo-6-deoxy-1,2-O-isopropylidene-5-O-p-nitrobenzoyl-β-L-idofuranose
CAS No.:131289-32-2
Molecular Formula:C₂₃H₂₂BrNO₉
Molecular Weight:536.333
Hs Code.:

Synonyms:3-O-benzoyl-6-bromo-6-deoxy-1,2-O-isopropylidene-5-O-p-nitrobenzoyl-β-L-idofuranose

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Chemical Property of 3-O-benzoyl-6-bromo-6-deoxy-1,2-O-isopropylidene-5-O-p-nitrobenzoyl-β-L-idofuranose

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Technology Process of 3-O-benzoyl-6-bromo-6-deoxy-1,2-O-isopropylidene-5-O-p-nitrobenzoyl-β-L-idofuranose

There total 1 articles about 3-O-benzoyl-6-bromo-6-deoxy-1,2-O-isopropylidene-5-O-p-nitrobenzoyl-β-L-idofuranose 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: 75.0%

: 95906-62-0
3,5-O-benzylidene-1,2-O-isopropylidene-α-D-glucofuranose 6-p-nitrobenzoate

: 131289-32-2
3-O-benzoyl-6-bromo-6-deoxy-1,2-O-isopropylidene-5-O-p-nitrobenzoyl-β-L-idofuranose

Guidance literature:: With N-Bromosuccinimide; barium carbonate; In tetrachloromethane; for 2.5h; Heating;
DOI:10.1016/0008-6215(90)80140-X

Reference yield: 72.3%

: 127-08-2
potassium acetate

: 131289-32-2
3-O-benzoyl-6-bromo-6-deoxy-1,2-O-isopropylidene-5-O-p-nitrobenzoyl-β-L-idofuranose

: 131289-33-3
6-O-acetyl-3-O-benzoyl-1,2-O-isopropylidene-5-O-p-nitrobenzoyl-β-L-idofuranose

Guidance literature:: With aluminum oxide; 18-crown-6 ether; In acetonitrile; for 6h; Heating;
DOI:10.1016/0008-6215(90)80140-X

Reference yield:

: 131289-32-2
3-O-benzoyl-6-bromo-6-deoxy-1,2-O-isopropylidene-5-O-p-nitrobenzoyl-β-L-idofuranose

: 26597-73-9,2847-00-9,26623-13-2,26623-14-3,26623-16-5
1,2:5,6-di-O-isopropylidene-α-D-glucofuranos-3-ulose

Guidance literature:: Multi-step reaction with 4 steps

1: 72.3 percent / activated alumina, 18-crown-6 / acetonitrile / 6 h / Heating

2: 0.1M sodium methoxide / methanol / 1 h / Ambient temperature

3: acetone

4: phosphorus pentaoxide / dimethylsulfoxide; dimethylformamide / 2.5 h / 65 °C

With aluminum oxide; phosphorus pentaoxide; 18-crown-6 ether; sodium methylate; In methanol; dimethyl sulfoxide; N,N-dimethyl-formamide; acetone; acetonitrile;
DOI:10.1016/0008-6215(90)80140-X