((1aR,2S,3aR,6R,7aS,7bS)-2-Methoxy-6-phenyl-hexahydro-3,5,7-trioxa-1-aza-cyclopropa[a]naphthalen-1-yl)-phenyl-methanone

Base Information

Chemical Name:((1aR,2S,3aR,6R,7aS,7bS)-2-Methoxy-6-phenyl-hexahydro-3,5,7-trioxa-1-aza-cyclopropa[a]naphthalen-1-yl)-phenyl-methanone
CAS No.:74841-91-1
Molecular Formula:C₂₁H₂₁NO₅
Molecular Weight:367.401
Hs Code.:

Synonyms:((1aR,2S,3aR,6R,7aS,7bS)-2-Methoxy-6-phenyl-hexahydro-3,5,7-trioxa-1-aza-cyclopropa[a]naphthalen-1-yl)-phenyl-methanone

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Chemical Property of ((1aR,2S,3aR,6R,7aS,7bS)-2-Methoxy-6-phenyl-hexahydro-3,5,7-trioxa-1-aza-cyclopropa[a]naphthalen-1-yl)-phenyl-methanone

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Technology Process of ((1aR,2S,3aR,6R,7aS,7bS)-2-Methoxy-6-phenyl-hexahydro-3,5,7-trioxa-1-aza-cyclopropa[a]naphthalen-1-yl)-phenyl-methanone

There total 4 articles about ((1aR,2S,3aR,6R,7aS,7bS)-2-Methoxy-6-phenyl-hexahydro-3,5,7-trioxa-1-aza-cyclopropa[a]naphthalen-1-yl)-phenyl-methanone 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:

: 74841-90-0
methyl 2-benzamido-4,6-O-benzylidene-2-deoxy-3-O-tosyl-α-D-glucopyranoside

: 74841-91-1
((1aR,2S,3aR,6R,7aS,7bS)-2-Methoxy-6-phenyl-hexahydro-3,5,7-trioxa-1-aza-cyclopropa[a]naphthalen-1-yl)-phenyl-methanone

Guidance literature:: With tetrabutyl ammonium fluoride; In N,N,N,N,N,N-hexamethylphosphoric triamide; at 85 ℃; for 0.0833333h;
DOI:10.1016/S0008-6215(00)85375-6

Reference yield:

: 131615-74-2
methyl 2-N-benzoylamido-4,6-O-benzylidene-2-deoxy-α-D-glucopyranoside

: 74841-91-1
((1aR,2S,3aR,6R,7aS,7bS)-2-Methoxy-6-phenyl-hexahydro-3,5,7-trioxa-1-aza-cyclopropa[a]naphthalen-1-yl)-phenyl-methanone

Guidance literature:: Multi-step reaction with 2 steps

1: 1.) TsCl, KOH, K₂CO₃, 2.) tetrabutylammonium hydrogen sulfate / 1.) toluene, DMSO, 30 min, 2.) 4 h

2: 89.8 percent / pyridine / 0.5 h

With potassium hydroxide; tetra(n-butyl)ammonium hydrogensulfate; potassium carbonate; p-toluenesulfonyl chloride; In pyridine;
DOI:10.1016/S0968-0896(98)00027-3

Reference yield:

: 1078691-95-8
(+)-D-glucosamine hydrochloride

: 74841-91-1
((1aR,2S,3aR,6R,7aS,7bS)-2-Methoxy-6-phenyl-hexahydro-3,5,7-trioxa-1-aza-cyclopropa[a]naphthalen-1-yl)-phenyl-methanone

Guidance literature:: Multi-step reaction with 3 steps

1: 1.) MeONa, 2.) H⁺, 3.) TsOH / 2.) MeOH, reflux, 3.) DMF, 50 deg C

2: 1.) TsCl, KOH, K₂CO₃, 2.) tetrabutylammonium hydrogen sulfate / 1.) toluene, DMSO, 30 min, 2.) 4 h

3: 89.8 percent / pyridine / 0.5 h

With potassium hydroxide; sodium methylate; tetra(n-butyl)ammonium hydrogensulfate; hydrogen cation; potassium carbonate; toluene-4-sulfonic acid; p-toluenesulfonyl chloride; In pyridine;
DOI:10.1016/S0968-0896(98)00027-3