tert-butyl benzyloxy(2-nitro-1-p-tolylethyl)carbamate

Base Information

Chemical Name:tert-butyl benzyloxy(2-nitro-1-p-tolylethyl)carbamate
CAS No.:1312926-12-7
Molecular Formula:C₂₁H₂₆N₂O₅
Molecular Weight:386.448
Hs Code.:

Synonyms:tert-butyl benzyloxy(2-nitro-1-p-tolylethyl)carbamate

Suppliers and Price of tert-butyl benzyloxy(2-nitro-1-p-tolylethyl)carbamate

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 tert-butyl benzyloxy(2-nitro-1-p-tolylethyl)carbamate

Chemical Property:

Purity/Quality:

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:

Useful:

Technology Process of tert-butyl benzyloxy(2-nitro-1-p-tolylethyl)carbamate

There total 2 articles about tert-butyl benzyloxy(2-nitro-1-p-tolylethyl)carbamate 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: 90.0%

: 7559-36-6,5153-68-4
4-methyl-β-nitrostyrene

: 79722-21-7
tert-butyl N-(benzyloxy)carbamate

: 1312926-12-7
tert-butyl benzyloxy(2-nitro-1-p-tolylethyl)carbamate

Guidance literature:: With Br^(1-)*C₁₁₇H₆₂F₄₈NO₂⁽¹⁺⁾; In water; toluene; at 0 ℃; for 36h; optical yield given as %ee; enantioselective reaction;
DOI:10.1002/anie.201101307

Reference yield:

: 7559-36-6,5153-68-4
4-methyl-β-nitrostyrene

: 79722-21-7
tert-butyl N-(benzyloxy)carbamate

: 1312926-12-7
tert-butyl benzyloxy(2-nitro-1-p-tolylethyl)carbamate

: C₂₁H₂₆N₂O₅

Guidance literature:: With C₂₉H₃₂F₆N₃O₂⁽¹⁺⁾*Br^(1-); In water; toluene; at 20 ℃; for 8h; Reagent/catalyst; Overall yield = 91 %; enantioselective reaction;
DOI:10.1039/c8ob00583d