tert-butyl (1R,2R)-2-(diethoxyphosphoryl)-2-(diphenylmethyleneamino)-1-(naphthalen-1-yl)ethylcarbamate

Base Information

Chemical Name:tert-butyl (1R,2R)-2-(diethoxyphosphoryl)-2-(diphenylmethyleneamino)-1-(naphthalen-1-yl)ethylcarbamate
CAS No.:1228746-87-9
Molecular Formula:C₃₄H₃₉N₂O₅P
Molecular Weight:586.668
Hs Code.:

Synonyms:tert-butyl (1R,2R)-2-(diethoxyphosphoryl)-2-(diphenylmethyleneamino)-1-(naphthalen-1-yl)ethylcarbamate

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

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Chemical Property of tert-butyl (1R,2R)-2-(diethoxyphosphoryl)-2-(diphenylmethyleneamino)-1-(naphthalen-1-yl)ethylcarbamate

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Technology Process of tert-butyl (1R,2R)-2-(diethoxyphosphoryl)-2-(diphenylmethyleneamino)-1-(naphthalen-1-yl)ethylcarbamate

There total 1 articles about tert-butyl (1R,2R)-2-(diethoxyphosphoryl)-2-(diphenylmethyleneamino)-1-(naphthalen-1-yl)ethylcarbamate 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: 85.0%

: 122570-91-6
diethyl N-(diphenylmethylene) aminomethyl phosphonate

: 479423-31-9
tert-butyl naphthalen-1-yl(phenylsulfonyl)methylcarbamate

: 1228746-87-9
tert-butyl (1R,2R)-2-(diethoxyphosphoryl)-2-(diphenylmethyleneamino)-1-(naphthalen-1-yl)ethylcarbamate

Guidance literature:: diethyl N-(diphenylmethylene) aminomethyl phosphonate; tert-butyl naphthalen-1-yl(phenylsulfonyl)methylcarbamate; With N-1-(oxy-pyridin-2-ylmethyl)quininium chloride; In tert-butyl methyl ether; toluene; at 20 ℃; for 0.0833333h;

With cesiumhydroxide monohydrate; In tert-butyl methyl ether; toluene; at -55 ℃; for 60h; optical yield given as %ee; diastereoselective reaction;
DOI:10.1002/adsc.200900208