N-((2R,4aR,6R,7R,8R,8aS)-8-Hydroxy-6-pent-4-enyloxy-2-phenyl-hexahydro-pyrano[3,2-d][1,3]dioxin-7-yl)-acetamide

Base Information

Chemical Name:N-((2R,4aR,6R,7R,8R,8aS)-8-Hydroxy-6-pent-4-enyloxy-2-phenyl-hexahydro-pyrano[3,2-d][1,3]dioxin-7-yl)-acetamide
CAS No.:824967-34-2
Molecular Formula:C₂₀H₂₇NO₆
Molecular Weight:377.437
Hs Code.:

Synonyms:N-((2R,4aR,6R,7R,8R,8aS)-8-Hydroxy-6-pent-4-enyloxy-2-phenyl-hexahydro-pyrano[3,2-d][1,3]dioxin-7-yl)-acetamide

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Chemical Property of N-((2R,4aR,6R,7R,8R,8aS)-8-Hydroxy-6-pent-4-enyloxy-2-phenyl-hexahydro-pyrano[3,2-d][1,3]dioxin-7-yl)-acetamide

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Technology Process of N-((2R,4aR,6R,7R,8R,8aS)-8-Hydroxy-6-pent-4-enyloxy-2-phenyl-hexahydro-pyrano[3,2-d][1,3]dioxin-7-yl)-acetamide

There total 4 articles about N-((2R,4aR,6R,7R,8R,8aS)-8-Hydroxy-6-pent-4-enyloxy-2-phenyl-hexahydro-pyrano[3,2-d][1,3]dioxin-7-yl)-acetamide 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: 82.0%

: 1125-88-8
benzaldehyde dimethyl acetal

: 128902-91-0
1-O-(4-penten-1-yl)-2-acetamido-2-deoxy-β-D-glucopyranoside

: 824967-34-2
N-((2R,4aR,6R,7R,8R,8aS)-8-Hydroxy-6-pent-4-enyloxy-2-phenyl-hexahydro-pyrano[3,2-d][1,3]dioxin-7-yl)-acetamide

Guidance literature:: With toluene-4-sulfonic acid; at 25 - 45 ℃; for 4h;
DOI:10.1016/j.tetlet.2014.11.029

Reference yield:

: 821-09-0
n-Pent-4-enyl alcohol

: 824967-34-2
N-((2R,4aR,6R,7R,8R,8aS)-8-Hydroxy-6-pent-4-enyloxy-2-phenyl-hexahydro-pyrano[3,2-d][1,3]dioxin-7-yl)-acetamide

Guidance literature:: Multi-step reaction with 3 steps

1: boron trifluoride diethyl etherate; trimethylsilyl trifluoromethanesulfonate / diethyl ether / 144 h / 25 - 45 °C

2: sodium methylate; methanol / 5 h / 25 °C

3: toluene-4-sulfonic acid / 4 h / 25 - 45 °C

With methanol; trimethylsilyl trifluoromethanesulfonate; boron trifluoride diethyl etherate; sodium methylate; toluene-4-sulfonic acid; In diethyl ether;
DOI:10.1016/j.tetlet.2014.11.029

Reference yield:

: 3006-60-8,4539-83-7,6730-10-5,7772-79-4,7784-54-5,10385-50-9,14086-90-9,26151-16-6,76375-60-5,76375-61-6,95341-98-3,95341-99-4,134451-91-5,134451-96-0,136982-81-5,145375-11-7,148347-15-3
2-acetamido-1,3,4,6-tetra-O-acetyl-2-deoxy-β-D-glucopyranose

: 824967-34-2
N-((2R,4aR,6R,7R,8R,8aS)-8-Hydroxy-6-pent-4-enyloxy-2-phenyl-hexahydro-pyrano[3,2-d][1,3]dioxin-7-yl)-acetamide

Guidance literature:: Multi-step reaction with 3 steps

1: boron trifluoride diethyl etherate; trimethylsilyl trifluoromethanesulfonate / diethyl ether / 144 h / 25 - 45 °C

2: sodium methylate; methanol / 5 h / 25 °C

3: toluene-4-sulfonic acid / 4 h / 25 - 45 °C

With methanol; trimethylsilyl trifluoromethanesulfonate; boron trifluoride diethyl etherate; sodium methylate; toluene-4-sulfonic acid; In diethyl ether;
DOI:10.1016/j.tetlet.2014.11.029