2,6-Anhydro-5-O-<4'-benzoyl>-3,4,7-tridesoxy-L-ribo-heptononitril

Base Information

Chemical Name:2,6-Anhydro-5-O-<4'-benzoyl>-3,4,7-tridesoxy-L-ribo-heptononitril
CAS No.:126257-46-3
Molecular Formula:C₂₇H₃₉NO₃
Molecular Weight:425.612
Hs Code.:

2,6-Anhydro-5-O-<4'-<trans-4''-(n-heptyl)cyclohexyl>benzoyl>-3,4,7-tridesoxy-L-ribo-heptononitril

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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 2,6-Anhydro-5-O-<4'-benzoyl>-3,4,7-tridesoxy-L-ribo-heptononitril

Chemical Property:

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Technology Process of 2,6-Anhydro-5-O-<4'-benzoyl>-3,4,7-tridesoxy-L-ribo-heptononitril

There total 5 articles about 2,6-Anhydro-5-O-<4'-benzoyl>-3,4,7-tridesoxy-L-ribo-heptononitril 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: 35.0%

: 126257-45-2
2,6-Anhydro-3,4,7-tridesoxy-L-ribo-heptononitril

: 81930-19-0
trans-4-(4-Heptylcyclohexyl)benzoesaeurechlorid

: 126257-46-3
2,6-Anhydro-5-O-<4'-benzoyl>-3,4,7-tridesoxy-L-ribo-heptononitril

Guidance literature:: With pyridine; for 1h;

Reference yield:

: 93978-97-3
4-O-acetyl-2,3,6-trideoxy-β-L-erythro-hex-2-enopyranosyl cyanide

: 126257-46-3
2,6-Anhydro-5-O-<4'-benzoyl>-3,4,7-tridesoxy-L-ribo-heptononitril

Guidance literature:: Multi-step reaction with 3 steps

1: 86 percent / H₂ / (Ph₃P)3RhCl / benzene / 760 Torr

2: 76 percent / KCN / methanol / 18 h / Ambient temperature

3: 35 percent / pyridine / 1 h

With pyridine; potassium cyanide; hydrogen; Wilkinson's catalyst; In methanol; benzene;

Reference yield:

: 34819-86-8
3,4-di-O-acetyl-6-deoxy-L-glucal

: 126257-46-3
2,6-Anhydro-5-O-<4'-benzoyl>-3,4,7-tridesoxy-L-ribo-heptononitril

Guidance literature:: Multi-step reaction with 4 steps

1: 47 percent / Et₂O*BF₃ / acetonitrile / 0.17 h

2: 86 percent / H₂ / (Ph₃P)3RhCl / benzene / 760 Torr

3: 76 percent / KCN / methanol / 18 h / Ambient temperature

4: 35 percent / pyridine / 1 h

With pyridine; potassium cyanide; boron trifluoride diethyl etherate; hydrogen; Wilkinson's catalyst; In methanol; acetonitrile; benzene;