7-ethyl-4-methyl-1-(4-nitro-phenyl)-2,6-dioxa-7-aza-bicyclo[2.2.2]octane

Base Information

Chemical Name:7-ethyl-4-methyl-1-(4-nitro-phenyl)-2,6-dioxa-7-aza-bicyclo[2.2.2]octane
CAS No.:266312-10-1
Molecular Formula:C₁₄H₁₈N₂O₄
Molecular Weight:278.308
Hs Code.:

Synonyms:7-ethyl-4-methyl-1-(4-nitro-phenyl)-2,6-dioxa-7-aza-bicyclo[2.2.2]octane

Suppliers and Price of 7-ethyl-4-methyl-1-(4-nitro-phenyl)-2,6-dioxa-7-aza-bicyclo[2.2.2]octane

Supply Marketing:

Business phase:: The product has achieved commercial mass production^*data from LookChem market partment

Manufacturers and distributors:

Manufacture/Brand
Chemicals and raw materials
Packaging
price

Total 0 raw suppliers

Chemical Property of 7-ethyl-4-methyl-1-(4-nitro-phenyl)-2,6-dioxa-7-aza-bicyclo[2.2.2]octane

Chemical Property:

Purity/Quality:

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:

Useful:

Technology Process of 7-ethyl-4-methyl-1-(4-nitro-phenyl)-2,6-dioxa-7-aza-bicyclo[2.2.2]octane

There total 5 articles about 7-ethyl-4-methyl-1-(4-nitro-phenyl)-2,6-dioxa-7-aza-bicyclo[2.2.2]octane 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:

: 266311-94-8
N-ethyl-N-(3-methyl-oxetan-3-ylmethyl)-4-nitro-benzamide

: 266312-10-1
7-ethyl-4-methyl-1-(4-nitro-phenyl)-2,6-dioxa-7-aza-bicyclo[2.2.2]octane

Guidance literature:: With boron trifluoride diethyl etherate; In chlorobenzene; at 120 - 130 ℃;
DOI:10.1016/S0040-4020(02)00701-9

Reference yield:

: 77-85-0
2-(hydroxymethyl)-2-methylpropane-1,3-diol

: 266312-10-1
7-ethyl-4-methyl-1-(4-nitro-phenyl)-2,6-dioxa-7-aza-bicyclo[2.2.2]octane

Guidance literature:: Multi-step reaction with 5 steps

1.1: (EtO)2CO; KOH

1.2: 64 percent / TsCl; aq. NaOH

2.1: N₂H₄*H₂O

2.2: 81 percent / Raney Ni (W-2)

4.1: K₂CO₃; NaOH; Bu₄NHSO₄

5.1: BF₃*OEt₂ / chlorobenzene / 130 °C

With potassium hydroxide; sodium hydroxide; boron trifluoride diethyl etherate; tetra(n-butyl)ammonium hydrogensulfate; potassium carbonate; hydrazine hydrate; Diethyl carbonate; In chlorobenzene; 1.1: Cyclization / 1.2: Substitution / 1.3: Substitution / 2.1: Substitution / 2.2: Reduction / 3.1: Acylation / 4.1: Alkylation / 5.1: Isomerization;
DOI:10.1021/jo991888g

Reference yield:

: 153209-97-3
(3-methyloxetan-3-yl)methanamine

: 266312-10-1
7-ethyl-4-methyl-1-(4-nitro-phenyl)-2,6-dioxa-7-aza-bicyclo[2.2.2]octane

Guidance literature:: Multi-step reaction with 3 steps

2: K₂CO₃; NaOH; Bu₄NHSO₄

3: BF₃*OEt₂ / chlorobenzene / 130 °C

With sodium hydroxide; boron trifluoride diethyl etherate; tetra(n-butyl)ammonium hydrogensulfate; potassium carbonate; In chlorobenzene; 1: Acylation / 2: Alkylation / 3: Isomerization;
DOI:10.1021/jo991888g