N-(trifluoroacetyl)glycine {N-benzyl-N-[4-ethoxycarbonyloxy-(2E)-buten-1-yl]}amide

Base Information

Chemical Name:N-(trifluoroacetyl)glycine {N-benzyl-N-[4-ethoxycarbonyloxy-(2E)-buten-1-yl]}amide
CAS No.:1599423-12-7
Molecular Formula:C₁₈H₂₁F₃N₂O₅
Molecular Weight:402.37
Hs Code.:

Synonyms:N-(trifluoroacetyl)glycine {N-benzyl-N-[4-ethoxycarbonyloxy-(2E)-buten-1-yl]}amide

Suppliers and Price of N-(trifluoroacetyl)glycine {N-benzyl-N-[4-ethoxycarbonyloxy-(2E)-buten-1-yl]}amide

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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 N-(trifluoroacetyl)glycine {N-benzyl-N-[4-ethoxycarbonyloxy-(2E)-buten-1-yl]}amide

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Technology Process of N-(trifluoroacetyl)glycine {N-benzyl-N-[4-ethoxycarbonyloxy-(2E)-buten-1-yl]}amide

There total 8 articles about N-(trifluoroacetyl)glycine {N-benzyl-N-[4-ethoxycarbonyloxy-(2E)-buten-1-yl]}amide 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: 96.0%

: 1599423-04-7
N-(trifluoroacetyl)glycine {N-benzyl-N-[4-hydroxy-(2E)-buten-1-yl]}amide

: 1599423-12-7
N-(trifluoroacetyl)glycine {N-benzyl-N-[4-ethoxycarbonyloxy-(2E)-buten-1-yl]}amide

Guidance literature:: With pyridine; In dichloromethane; at 0 - 20 ℃; Inert atmosphere;
DOI:10.1002/ejoc.201301659

Reference yield: 96.0%

: 1599423-04-7
N-(trifluoroacetyl)glycine {N-benzyl-N-[4-hydroxy-(2E)-buten-1-yl]}amide

: 541-41-3
chloroformic acid ethyl ester

: 1599423-12-7
N-(trifluoroacetyl)glycine {N-benzyl-N-[4-ethoxycarbonyloxy-(2E)-buten-1-yl]}amide

Guidance literature:: With pyridine; In dichloromethane; at 0 ℃;
DOI:10.1002/ejoc.201301659

Reference yield:

: 1099751-95-7
(2E)-N-benzyl-4-(tert-butyldimethylsiloxy)but-2-en-1-amine

: 1599423-12-7
N-(trifluoroacetyl)glycine {N-benzyl-N-[4-ethoxycarbonyloxy-(2E)-buten-1-yl]}amide

Guidance literature:: Multi-step reaction with 3 steps

1: N-ethyl-N,N-diisopropylamine; 2-bromo-1-ethylpyridin-1-ium tetrafluoroborate / dichloromethane / -10 - 20 °C / Inert atmosphere

2: tetrabutyl ammonium fluoride / tetrahydrofuran / 0.5 h

3: pyridine / dichloromethane / 0 - 20 °C / Inert atmosphere

With pyridine; tetrabutyl ammonium fluoride; 2-bromo-1-ethylpyridin-1-ium tetrafluoroborate; N-ethyl-N,N-diisopropylamine; In tetrahydrofuran; dichloromethane;
DOI:10.1002/ejoc.201301659