1-Benzyl-3-((3aR,4R,6R,6aR)-6-hydroxymethyl-2,2-dimethyl-tetrahydro-furo[3,4-d][1,3]dioxol-4-yl)-5-methyl-3-phenylselanyl-piperidine-2,6-dione

Base Information

• Chemical Name: 1-Benzyl-3-((3aR,4R,6R,6aR)-6-hydroxymethyl-2,2-dimethyl-tetrahydro-furo[3,4-d][1,3]dioxol-4-yl)-5-methyl-3-phenylselanyl-piperidine-2,6-dione
• CAS No.: 129420-95-7
• Molecular Formula: C₂₇H₃₁NO₆Se
• Molecular Weight: 544.506
• Mol file: 129420-95-7.mol

Synonyms:

Chemical Property of 1-Benzyl-3-((3aR,4R,6R,6aR)-6-hydroxymethyl-2,2-dimethyl-tetrahydro-furo[3,4-d][1,3]dioxol-4-yl)-5-methyl-3-phenylselanyl-piperidine-2,6-dione

Chemical Property:

Purity/Quality:

Safty Information:

• Pictogram(s):  
• Hazard Codes: 

MSDS Files:

Useful:

Technology Process of 1-Benzyl-3-((3aR,4R,6R,6aR)-6-hydroxymethyl-2,2-dimethyl-tetrahydro-furo[3,4-d][1,3]dioxol-4-yl)-5-methyl-3-phenylselanyl-piperidine-2,6-dione

There total 4 articles about 1-Benzyl-3-((3aR,4R,6R,6aR)-6-hydroxymethyl-2,2-dimethyl-tetrahydro-furo[3,4-d][1,3]dioxol-4-yl)-5-methyl-3-phenylselanyl-piperidine-2,6-dione 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: 41.0%

Phenylselenyl chloride (5707-04-0) + 1-Benzyl-3-[1-[(4S,5R)-5-((R)-1-hydroxy-2-trityloxy-ethyl)-2,2-dimethyl-[1,3]dioxolan-4-yl]-meth-(Z)-ylidene]-5-methyl-piperidine-2,6-dione (129395-69-3,129445-96-1,129445-97-2,129445-98-3) → 1-Benzyl-3-((3aR,4R,6R,6aR)-6-hydroxymethyl-2,2-dimethyl-tetrahydro-furo[3,4-d][1,3]dioxol-4-yl)-5-methyl-3-phenylselanyl-piperidine-2,6-dione (129420-95-7)

Guidance literature:

In acetonitrile; for 6h; Ambient temperature;

DOI:10.1016/S0040-4039(00)94660-4

Reference yield:

N-Benzyl-2-(triphenyl-λ5-phosphanylidene)-acetamide (129395-67-1) → 1-Benzyl-3-((3aR,4R,6R,6aR)-6-hydroxymethyl-2,2-dimethyl-tetrahydro-furo[3,4-d][1,3]dioxol-4-yl)-5-methyl-3-phenylselanyl-piperidine-2,6-dione (129420-95-7)

Guidance literature:

Multi-step reaction with 3 steps

1: 22 percent / methanol / 1) 16h, room temperature 2) 3h, reflux

2: 53 percent / toluene / 30 h / Heating

3: 41 percent / acetonitrile / 6 h / Ambient temperature

In methanol; toluene; acetonitrile;

DOI:10.1016/S0040-4039(00)94660-4

Reference yield:

2,3-O-isopropylidene-5-O-trityl-D-ribofuranose (54503-64-9,54503-65-0) → 1-Benzyl-3-((3aR,4R,6R,6aR)-6-hydroxymethyl-2,2-dimethyl-tetrahydro-furo[3,4-d][1,3]dioxol-4-yl)-5-methyl-3-phenylselanyl-piperidine-2,6-dione (129420-95-7)

Guidance literature:

Multi-step reaction with 2 steps

1: 53 percent / toluene / 30 h / Heating

2: 41 percent / acetonitrile / 6 h / Ambient temperature

In toluene; acetonitrile;

DOI:10.1016/S0040-4039(00)94660-4

upstream raw materials:

Phenylselenyl chloride

1-Benzyl-3-[1-[(4S,5R)-5-((R)-1-hydroxy-2-trityloxy-ethyl)-2,2-dimethyl-[1,3]dioxolan-4-yl]-meth-(Z)-ylidene]-5-methyl-piperidine-2,6-dione

N-Benzyl-2-(triphenyl-λ⁵-phosphanylidene)-acetamide

2,3-O-isopropylidene-5-O-trityl-D-ribofuranose