N-[(1S,2S)-2-((S)-1-Allyl-nonyloxy)-1-methyl-2-phenyl-ethyl]-2,2,2-trifluoro-acetamide

Base Information

Chemical Name:N-[(1S,2S)-2-((S)-1-Allyl-nonyloxy)-1-methyl-2-phenyl-ethyl]-2,2,2-trifluoro-acetamide
CAS No.:183509-49-1
Molecular Formula:C₂₃H₃₄F₃NO₂
Molecular Weight:413.524
Hs Code.:

Synonyms:N-[(1S,2S)-2-((S)-1-Allyl-nonyloxy)-1-methyl-2-phenyl-ethyl]-2,2,2-trifluoro-acetamide

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Chemical Property of N-[(1S,2S)-2-((S)-1-Allyl-nonyloxy)-1-methyl-2-phenyl-ethyl]-2,2,2-trifluoro-acetamide

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Technology Process of N-[(1S,2S)-2-((S)-1-Allyl-nonyloxy)-1-methyl-2-phenyl-ethyl]-2,2,2-trifluoro-acetamide

There total 3 articles about N-[(1S,2S)-2-((S)-1-Allyl-nonyloxy)-1-methyl-2-phenyl-ethyl]-2,2,2-trifluoro-acetamide 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:

: 2153-98-2
(-)-Norpseudoephedrine hydrochloride

: 183509-49-1
N-[(1S,2S)-2-((S)-1-Allyl-nonyloxy)-1-methyl-2-phenyl-ethyl]-2,2,2-trifluoro-acetamide

Guidance literature:: Multi-step reaction with 3 steps

1: Et₃N / methanol / 18 h / Ambient temperature

2: Et₃N / CH₂Cl₂ / 4 h / Ambient temperature

3: 1.) TMSOTf / 1.) CH₂Cl₂, -78 deg C, 1 h, 2.) CH₂Cl₂, 48 h

With trimethylsilyl trifluoromethanesulfonate; triethylamine; In methanol; dichloromethane;

Reference yield:

: 2,2,2-Trifluoro-N-((1S,2S)-2-hydroxy-1-methyl-2-phenyl-ethyl)-acetamide

: 183509-49-1
N-[(1S,2S)-2-((S)-1-Allyl-nonyloxy)-1-methyl-2-phenyl-ethyl]-2,2,2-trifluoro-acetamide

Guidance literature:: Multi-step reaction with 2 steps

1: Et₃N / CH₂Cl₂ / 4 h / Ambient temperature

2: 1.) TMSOTf / 1.) CH₂Cl₂, -78 deg C, 1 h, 2.) CH₂Cl₂, 48 h

With trimethylsilyl trifluoromethanesulfonate; triethylamine; In dichloromethane;

Reference yield:

: 124-19-6
nonan-1-al

: 183378-05-4
trimethylsilyl ether of (1S,2S)-N-trifluoroacetamidonorpseudoephedrine

: 762-72-1
allyl-trimethyl-silane

: 183509-49-1
N-[(1S,2S)-2-((S)-1-Allyl-nonyloxy)-1-methyl-2-phenyl-ethyl]-2,2,2-trifluoro-acetamide

Guidance literature:: With trimethylsilyl trifluoromethanesulfonate; Yield given. Multistep reaction; 1.) CH₂Cl₂, -78 deg C, 1 h, 2.) CH₂Cl₂, 48 h;