methyl 4,6-O-(phenylmethylene)-3-deoxy-2-O-methyl-3-(4-morpholinyl)-α-D-altro-pyranoside

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Chemical Name:methyl 4,6-O-(phenylmethylene)-3-deoxy-2-O-methyl-3-(4-morpholinyl)-α-D-altro-pyranoside
CAS No.:256455-96-6
Molecular Formula:C₁₉H₂₇NO₆
Molecular Weight:365.426
Hs Code.:

Synonyms:methyl 4,6-O-(phenylmethylene)-3-deoxy-2-O-methyl-3-(4-morpholinyl)-α-D-altro-pyranoside

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Chemical Property of methyl 4,6-O-(phenylmethylene)-3-deoxy-2-O-methyl-3-(4-morpholinyl)-α-D-altro-pyranoside

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Technology Process of methyl 4,6-O-(phenylmethylene)-3-deoxy-2-O-methyl-3-(4-morpholinyl)-α-D-altro-pyranoside

There total 2 articles about methyl 4,6-O-(phenylmethylene)-3-deoxy-2-O-methyl-3-(4-morpholinyl)-α-D-altro-pyranoside 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: 86.0%

: 256455-94-4
methyl 4,6-O-(phenylmethylene)-3-deoxy-3-(4-morpholinyl)-α-D-altro-pyranoside

: 74-88-4
methyl iodide

: 256455-96-6
methyl 4,6-O-(phenylmethylene)-3-deoxy-2-O-methyl-3-(4-morpholinyl)-α-D-altro-pyranoside

Guidance literature:: methyl 4,6-O-(phenylmethylene)-3-deoxy-3-(4-morpholinyl)-α-D-altro-pyranoside; With sodium hydride; In 1,4-dioxane; at 20 ℃; for 0.5h;

methyl iodide; In 1,4-dioxane; at 20 ℃; for 26h;
DOI:10.1021/jo982199s

Reference yield:

: 3150-15-0,3150-16-1,3257-59-8,14187-71-4,15384-57-3,19465-13-5,32976-15-1,52885-37-7,53270-02-3,53270-03-4,65391-11-9,65391-12-0,66537-92-6,67226-04-4,71184-14-0,86420-78-2,86420-79-3,91177-51-4,91177-52-5,117708-93-7,120408-72-2,2880-96-8
methyl 2,3-anhydro-4,6-O-benzilidene-α-D-mannopyranoside

: 256455-96-6
methyl 4,6-O-(phenylmethylene)-3-deoxy-2-O-methyl-3-(4-morpholinyl)-α-D-altro-pyranoside

Guidance literature:: Multi-step reaction with 2 steps

1.1: 89 percent / 10 h / 90 - 100 °C

2.1: NaH / dioxane / 0.5 h / 20 °C

2.2: 86 percent / dioxane / 26 h / 20 °C

With sodium hydride; In 1,4-dioxane; 1.1: Ring cleavage / 2.1: deprotonation / 2.2: Methylation;
DOI:10.1021/jo982199s