((3aR,6S,6aS)-2,2-Dimethyl-6-trityloxymethyl-tetrahydro-furo[3,4-d][1,3]dioxol-4-yl)-acetonitrile

Base Information

Chemical Name:((3aR,6S,6aS)-2,2-Dimethyl-6-trityloxymethyl-tetrahydro-furo[3,4-d][1,3]dioxol-4-yl)-acetonitrile
CAS No.:196101-51-6
Molecular Formula:C₂₉H₂₉NO₄
Molecular Weight:455.554
Hs Code.:

Synonyms:((3aR,6S,6aS)-2,2-Dimethyl-6-trityloxymethyl-tetrahydro-furo[3,4-d][1,3]dioxol-4-yl)-acetonitrile

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Chemical Property of ((3aR,6S,6aS)-2,2-Dimethyl-6-trityloxymethyl-tetrahydro-furo[3,4-d][1,3]dioxol-4-yl)-acetonitrile

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Technology Process of ((3aR,6S,6aS)-2,2-Dimethyl-6-trityloxymethyl-tetrahydro-furo[3,4-d][1,3]dioxol-4-yl)-acetonitrile

There total 4 articles about ((3aR,6S,6aS)-2,2-Dimethyl-6-trityloxymethyl-tetrahydro-furo[3,4-d][1,3]dioxol-4-yl)-acetonitrile 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:

: 171721-11-2
5-O-benzoyl-1,2-O-isopropylidene-α-L-ribofuranose

: 196101-51-6
((3aR,6S,6aS)-2,2-Dimethyl-6-trityloxymethyl-tetrahydro-furo[3,4-d][1,3]dioxol-4-yl)-acetonitrile

Guidance literature:: Multi-step reaction with 5 steps

1: formic acid / 16 h / Ambient temperature

2: H₂SO₄ / acetone / 2 h / Ambient temperature

3: 92.8 percent / NaOH / methanol / 6 h / Ambient temperature

4: 87.9 percent / Py / 6 h / 80 °C

5: 1.) NaH / 1.) DME, 0 deg C, 20 min, 2.) DME, room temperature, 2 h.

With pyridine; sodium hydroxide; formic acid; sulfuric acid; sodium hydride; In methanol; acetone;
DOI:10.1016/S0008-6215(97)00143-2

Reference yield:

: 5-O-benzoyl-L-ribofuranose

: 196101-51-6
((3aR,6S,6aS)-2,2-Dimethyl-6-trityloxymethyl-tetrahydro-furo[3,4-d][1,3]dioxol-4-yl)-acetonitrile

Guidance literature:: Multi-step reaction with 4 steps

1: H₂SO₄ / acetone / 2 h / Ambient temperature

2: 92.8 percent / NaOH / methanol / 6 h / Ambient temperature

3: 87.9 percent / Py / 6 h / 80 °C

4: 1.) NaH / 1.) DME, 0 deg C, 20 min, 2.) DME, room temperature, 2 h.

With pyridine; sodium hydroxide; sulfuric acid; sodium hydride; In methanol; acetone;
DOI:10.1016/S0008-6215(97)00143-2

Reference yield:

: 5-O-benzoyl-2,3-O-isopropylidene-L-ribofuranose

: 196101-51-6
((3aR,6S,6aS)-2,2-Dimethyl-6-trityloxymethyl-tetrahydro-furo[3,4-d][1,3]dioxol-4-yl)-acetonitrile

Guidance literature:: Multi-step reaction with 3 steps

1: 92.8 percent / NaOH / methanol / 6 h / Ambient temperature

2: 87.9 percent / Py / 6 h / 80 °C

3: 1.) NaH / 1.) DME, 0 deg C, 20 min, 2.) DME, room temperature, 2 h.

With pyridine; sodium hydroxide; sodium hydride; In methanol;
DOI:10.1016/S0008-6215(97)00143-2