tert-butyl (3S,αR)-3-[N-benzyl-N-(α-methylbenzyl)amino]-3-(2',3'-difluorophenyl)propanoate

Base Information

Chemical Name:tert-butyl (3S,αR)-3-[N-benzyl-N-(α-methylbenzyl)amino]-3-(2',3'-difluorophenyl)propanoate
CAS No.:1393363-60-4
Molecular Formula:C₂₈H₃₁F₂NO₂
Molecular Weight:451.556
Hs Code.:

Synonyms:tert-butyl (3S,αR)-3-[N-benzyl-N-(α-methylbenzyl)amino]-3-(2',3'-difluorophenyl)propanoate

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Chemical Property of tert-butyl (3S,αR)-3-[N-benzyl-N-(α-methylbenzyl)amino]-3-(2',3'-difluorophenyl)propanoate

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Technology Process of tert-butyl (3S,αR)-3-[N-benzyl-N-(α-methylbenzyl)amino]-3-(2',3'-difluorophenyl)propanoate

There total 2 articles about tert-butyl (3S,αR)-3-[N-benzyl-N-(α-methylbenzyl)amino]-3-(2',3'-difluorophenyl)propanoate 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: 84.0%

: 1393363-50-2
tert-butyl (E)-3-(2',3'-difluorophenyl)prop-2-enoate

: 38235-77-7
(R)-N-benzyl-1-phenylethylamine

: 1393363-60-4
tert-butyl (3S,αR)-3-[N-benzyl-N-(α-methylbenzyl)amino]-3-(2',3'-difluorophenyl)propanoate

Guidance literature:: (R)-N-benzyl-1-phenylethylamine; With n-butyllithium; In tetrahydrofuran; hexane; at -78 ℃; for 0.5h; Inert atmosphere;

tert-butyl (E)-3-(2',3'-difluorophenyl)prop-2-enoate; In tetrahydrofuran; hexane; at -78 ℃; for 2h; Inert atmosphere;

With ammonium chloride; In tetrahydrofuran; hexane; water; at -78 - 20 ℃; optical yield given as %de; diastereoselective reaction; Saturated solution;
DOI:10.1016/j.tetasy.2012.07.001

Reference yield:

: 27784-76-5
tert-butyl diethylphosphonoacetate

: 1393363-60-4
tert-butyl (3S,αR)-3-[N-benzyl-N-(α-methylbenzyl)amino]-3-(2',3'-difluorophenyl)propanoate

Guidance literature:: Multi-step reaction with 2 steps

1.1: methylmagnesium bromide / tetrahydrofuran; diethyl ether / 0.25 h / 20 °C / Inert atmosphere

1.2: 15 h / Inert atmosphere; Reflux

2.1: n-butyllithium / tetrahydrofuran; hexane / 0.5 h / -78 °C / Inert atmosphere

2.2: 2 h / -78 °C / Inert atmosphere

2.3: -78 - 20 °C / Saturated solution

With n-butyllithium; methylmagnesium bromide; In tetrahydrofuran; diethyl ether; hexane; 1.2: Horner-Wadsworth-Emmons olefination;
DOI:10.1016/j.tetasy.2012.07.001