1,5-anhydro-2-deoxy-3-O-{2,4,6-tri-O-benzoyl-3-O-[(1S)-1-(cyclohexylmethyl)-2-oxo-2-(phenylmethoxy)ethyl]-β-D-galactopyranosyl}-D-arabino-hexitol

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Chemical Name:1,5-anhydro-2-deoxy-3-O-{2,4,6-tri-O-benzoyl-3-O-[(1S)-1-(cyclohexylmethyl)-2-oxo-2-(phenylmethoxy)ethyl]-β-D-galactopyranosyl}-D-arabino-hexitol
CAS No.:322761-82-0
Molecular Formula:C₄₉H₅₄O₁₄
Molecular Weight:866.959
Hs Code.:

Synonyms:1,5-anhydro-2-deoxy-3-O-{2,4,6-tri-O-benzoyl-3-O-[(1S)-1-(cyclohexylmethyl)-2-oxo-2-(phenylmethoxy)ethyl]-β-D-galactopyranosyl}-D-arabino-hexitol

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Chemical Property of 1,5-anhydro-2-deoxy-3-O-{2,4,6-tri-O-benzoyl-3-O-[(1S)-1-(cyclohexylmethyl)-2-oxo-2-(phenylmethoxy)ethyl]-β-D-galactopyranosyl}-D-arabino-hexitol

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Technology Process of 1,5-anhydro-2-deoxy-3-O-{2,4,6-tri-O-benzoyl-3-O-[(1S)-1-(cyclohexylmethyl)-2-oxo-2-(phenylmethoxy)ethyl]-β-D-galactopyranosyl}-D-arabino-hexitol

There total 6 articles about 1,5-anhydro-2-deoxy-3-O-{2,4,6-tri-O-benzoyl-3-O-[(1S)-1-(cyclohexylmethyl)-2-oxo-2-(phenylmethoxy)ethyl]-β-D-galactopyranosyl}-D-arabino-hexitol 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:

: 135214-83-4
1,5-Anhydro-2-deoxy-4,6-O-(phenylmethylene)-D-arabino-hexopyranoside

: 322761-82-0
1,5-anhydro-2-deoxy-3-O-{2,4,6-tri-O-benzoyl-3-O-[(1S)-1-(cyclohexylmethyl)-2-oxo-2-(phenylmethoxy)ethyl]-β-D-galactopyranosyl}-D-arabino-hexitol

Guidance literature:: Multi-step reaction with 2 steps

1: CF₃SO₃H; N-iodosuccinimide / CH₂Cl₂ / -10 °C

2: 9.03 g / AcOH / H₂O / Heating

With N-iodo-succinimide; trifluorormethanesulfonic acid; acetic acid; In dichloromethane; water;
DOI:10.1002/1522-2675(20001108)83:11<2893::AID-HLCA2893>3.0.CO;2-G

Reference yield:

: 98-88-4
benzoyl chloride

: 322761-82-0
1,5-anhydro-2-deoxy-3-O-{2,4,6-tri-O-benzoyl-3-O-[(1S)-1-(cyclohexylmethyl)-2-oxo-2-(phenylmethoxy)ethyl]-β-D-galactopyranosyl}-D-arabino-hexitol

Guidance literature:: Multi-step reaction with 3 steps

1: 90 percent / DMAP / pyridine / 6 h / 20 °C

2: CF₃SO₃H; N-iodosuccinimide / CH₂Cl₂ / -10 °C

3: 9.03 g / AcOH / H₂O / Heating

With dmap; N-iodo-succinimide; trifluorormethanesulfonic acid; acetic acid; In pyridine; dichloromethane; water;
DOI:10.1002/1522-2675(20001108)83:11<2893::AID-HLCA2893>3.0.CO;2-G

Reference yield:

: 187404-16-6
benzyl (R)-3-cyclohexyl-2-trifluoromethanesulfonyloxy-propionate

: 322761-82-0
1,5-anhydro-2-deoxy-3-O-{2,4,6-tri-O-benzoyl-3-O-[(1S)-1-(cyclohexylmethyl)-2-oxo-2-(phenylmethoxy)ethyl]-β-D-galactopyranosyl}-D-arabino-hexitol

Guidance literature:: Multi-step reaction with 4 steps

1.1: Bu₂SnO / methanol / 2 h / Heating

1.2: 65 percent / CsF / 1,2-dimethoxy-ethane / 2 h / 20 °C

2.1: 90 percent / DMAP / pyridine / 6 h / 20 °C

3.1: CF₃SO₃H; N-iodosuccinimide / CH₂Cl₂ / -10 °C

4.1: 9.03 g / AcOH / H₂O / Heating

With dmap; N-iodo-succinimide; trifluorormethanesulfonic acid; di(n-butyl)tin oxide; acetic acid; In pyridine; methanol; dichloromethane; water;
DOI:10.1002/1522-2675(20001108)83:11<2893::AID-HLCA2893>3.0.CO;2-G