benzyl N-{1-[bis(2,2,2-trifluoroethoxy)phosphoryl]-2-phenylethyl}carbamate

Base Information

Chemical Name:benzyl N-{1-[bis(2,2,2-trifluoroethoxy)phosphoryl]-2-phenylethyl}carbamate
CAS No.:174298-12-5
Molecular Formula:C₂₀H₂₀F₆NO₅P
Molecular Weight:499.347
Hs Code.:

Synonyms:benzyl N-{1-[bis(2,2,2-trifluoroethoxy)phosphoryl]-2-phenylethyl}carbamate

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Chemical Property of benzyl N-{1-[bis(2,2,2-trifluoroethoxy)phosphoryl]-2-phenylethyl}carbamate

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Technology Process of benzyl N-{1-[bis(2,2,2-trifluoroethoxy)phosphoryl]-2-phenylethyl}carbamate

There total 2 articles about benzyl N-{1-[bis(2,2,2-trifluoroethoxy)phosphoryl]-2-phenylethyl}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: 31.0%

: 621-84-1
O-benzyl carbamate

: 122-78-1
phenylacetaldehyde

: 92466-70-1
bis(2,2,2-trifluoroethyl)phosphite

: 174298-12-5
benzyl N-{1-[bis(2,2,2-trifluoroethoxy)phosphoryl]-2-phenylethyl}carbamate

Guidance literature:: With acetic anhydride; trifluoroacetic acid; at 20 ℃; for 24h;
DOI:10.1016/j.tetlet.2013.01.039

Reference yield: 18.0%

: 370-69-4
tris(2,2,2-trifluoroethyl)phosphite

: 621-84-1
O-benzyl carbamate

: 122-78-1
phenylacetaldehyde

: 174298-12-5
benzyl N-{1-[bis(2,2,2-trifluoroethoxy)phosphoryl]-2-phenylethyl}carbamate

Guidance literature:: With acetic acid; for 4h; Reflux;
DOI:10.1016/j.tetlet.2013.01.039

Reference yield:

: 174298-12-5
benzyl N-{1-[bis(2,2,2-trifluoroethoxy)phosphoryl]-2-phenylethyl}carbamate

: 1423779-06-9
tert-butyl N-{(2S)-1-[(2S)-2-({1-[bis(2,2,2-trifluoroethoxy)phosphoryl]-2-phenylethyl}carbamoyl)pyrrolidin-1-yl]-3-methyl-1-oxobutan-2-yl}carbamate

Guidance literature:: Multi-step reaction with 2 steps

1: acetic acid; hydrogen bromide

2: N-ethyl-N,N-diisopropylamine; O-(1H-benzotriazol-1-yl)-N,N,N',N'-tetramethyluronium hexafluorophosphate / acetonitrile / 24 h / 20 °C

With hydrogen bromide; O-(1H-benzotriazol-1-yl)-N,N,N',N'-tetramethyluronium hexafluorophosphate; acetic acid; N-ethyl-N,N-diisopropylamine; In acetonitrile;
DOI:10.1016/j.tetlet.2013.01.039