N-tert-butoxycarbonyl-N-[o-(1,1-difluorohex-1-en-2-yl)benzyl]-p-toluenesulfonamide

Base Information

Chemical Name:N-tert-butoxycarbonyl-N-[o-(1,1-difluorohex-1-en-2-yl)benzyl]-p-toluenesulfonamide
CAS No.:259152-15-3
Molecular Formula:C₂₅H₃₁F₂NO₄S
Molecular Weight:479.588
Hs Code.:

Synonyms:N-tert-butoxycarbonyl-N-[o-(1,1-difluorohex-1-en-2-yl)benzyl]-p-toluenesulfonamide

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Chemical Property of N-tert-butoxycarbonyl-N-[o-(1,1-difluorohex-1-en-2-yl)benzyl]-p-toluenesulfonamide

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Technology Process of N-tert-butoxycarbonyl-N-[o-(1,1-difluorohex-1-en-2-yl)benzyl]-p-toluenesulfonamide

There total 3 articles about N-tert-butoxycarbonyl-N-[o-(1,1-difluorohex-1-en-2-yl)benzyl]-p-toluenesulfonamide 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: 83.0%

: 18303-04-3
N-[(tert-butoxy)carbonyl]-4-methylbenzenesulfonamide

: 353238-07-0
2-(1-butyl-2,2-difluorovinyl)benzyl alcohol

: 259152-15-3
N-tert-butoxycarbonyl-N-[o-(1,1-difluorohex-1-en-2-yl)benzyl]-p-toluenesulfonamide

Guidance literature:: With triphenylphosphine; diethylazodicarboxylate; In tetrahydrofuran; at 20 ℃; for 1h;
DOI:10.1055/s-2006-926458

Reference yield:

: C₁₁H₁₅IMgO

: 259152-15-3
N-tert-butoxycarbonyl-N-[o-(1,1-difluorohex-1-en-2-yl)benzyl]-p-toluenesulfonamide

Guidance literature:: Multi-step reaction with 2 steps

1: 69 percent / CuI; Ph₃P / Pd₂(dba)3*CHCl₃ / tetrahydrofuran; hexamethylphosphoric acid triamide / 17 h / 20 °C

2: 83 percent / Ph₃P; diethyl azodicarboxylate / tetrahydrofuran / 1 h / 20 °C

With copper(l) iodide; triphenylphosphine; diethylazodicarboxylate; tris(dibenzylideneacetone)dipalladium⁽⁰⁾ chloroform complex; In tetrahydrofuran; N,N,N,N,N,N-hexamethylphosphoric triamide; 2: Mitsunobu reaction;
DOI:10.1055/s-2006-926458

Reference yield:

: 134810-60-9
dibutyl-(1-butyl-2,2-difluoro-vinyl)-borane

: 259152-15-3
N-tert-butoxycarbonyl-N-[o-(1,1-difluorohex-1-en-2-yl)benzyl]-p-toluenesulfonamide

Guidance literature:: Multi-step reaction with 2 steps

1: 69 percent / CuI; Ph₃P / Pd₂(dba)3*CHCl₃ / tetrahydrofuran; hexamethylphosphoric acid triamide / 17 h / 20 °C

2: 83 percent / Ph₃P; diethyl azodicarboxylate / tetrahydrofuran / 1 h / 20 °C

With copper(l) iodide; triphenylphosphine; diethylazodicarboxylate; tris(dibenzylideneacetone)dipalladium⁽⁰⁾ chloroform complex; In tetrahydrofuran; N,N,N,N,N,N-hexamethylphosphoric triamide; 2: Mitsunobu reaction;
DOI:10.1055/s-2006-926458