(R)-2,3-epoxypropyl 4,6-O-benzylidene-2-deoxy-2-hexanamido-β-D-glucopyranoside

Base Information

Chemical Name:(R)-2,3-epoxypropyl 4,6-O-benzylidene-2-deoxy-2-hexanamido-β-D-glucopyranoside
CAS No.:321679-25-8
Molecular Formula:C₂₂H₃₁NO₇
Molecular Weight:421.491
Hs Code.:

Synonyms:(R)-2,3-epoxypropyl 4,6-O-benzylidene-2-deoxy-2-hexanamido-β-D-glucopyranoside

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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 (R)-2,3-epoxypropyl 4,6-O-benzylidene-2-deoxy-2-hexanamido-β-D-glucopyranoside

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Technology Process of (R)-2,3-epoxypropyl 4,6-O-benzylidene-2-deoxy-2-hexanamido-β-D-glucopyranoside

There total 4 articles about (R)-2,3-epoxypropyl 4,6-O-benzylidene-2-deoxy-2-hexanamido-β-D-glucopyranoside 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: 76.0%

: 321679-21-4
allyl 4,6-O-benzylidene-2-deoxy-2-hexanamido-β-D-glucopyranoside

: 321679-25-8
(R)-2,3-epoxypropyl 4,6-O-benzylidene-2-deoxy-2-hexanamido-β-D-glucopyranoside

Guidance literature:: With sodium sulfate; 3-chloro-benzenecarboperoxoic acid; In chloroform; at 20 ℃;
DOI:10.1002/1099-0690(200012)2000:23<3949::AID-EJOC3949>3.0.CO;2-J

Reference yield:

: 63064-49-3,65947-37-7,74984-84-2,88903-98-4,92841-84-4,116347-88-7,136845-44-8,138456-61-8,74984-83-1
allyl 2-acetamido-(R)-4,6-O-benzylidene-2-deoxy-β-D-glucopyranoside

: 321679-25-8
(R)-2,3-epoxypropyl 4,6-O-benzylidene-2-deoxy-2-hexanamido-β-D-glucopyranoside

Guidance literature:: Multi-step reaction with 4 steps

1: potassium hydroxide / ethanol / 6 h / Heating

2: 6.9 g / pyridine / 20 °C

3: 90 percent / sodium methoxide / methanol / 0.5 h / 20 °C

4: 76 percent / sodium sulfate; m-chloroperoxybenzoic acid / CHCl₃ / 20 °C

With pyridine; potassium hydroxide; sodium methylate; sodium sulfate; 3-chloro-benzenecarboperoxoic acid; In methanol; ethanol; chloroform;
DOI:10.1002/1099-0690(200012)2000:23<3949::AID-EJOC3949>3.0.CO;2-J

Reference yield:

: 913258-78-3
(2R,4aR,6R,7R,8R,8aS)-6-Allyloxy-7-amino-2-phenyl-hexahydro-pyrano[3,2-d][1,3]dioxin-8-ol

: 321679-25-8
(R)-2,3-epoxypropyl 4,6-O-benzylidene-2-deoxy-2-hexanamido-β-D-glucopyranoside

Guidance literature:: Multi-step reaction with 3 steps

1: 6.9 g / pyridine / 20 °C

2: 90 percent / sodium methoxide / methanol / 0.5 h / 20 °C

3: 76 percent / sodium sulfate; m-chloroperoxybenzoic acid / CHCl₃ / 20 °C

With pyridine; sodium methylate; sodium sulfate; 3-chloro-benzenecarboperoxoic acid; In methanol; chloroform;
DOI:10.1002/1099-0690(200012)2000:23<3949::AID-EJOC3949>3.0.CO;2-J