tert-butyl [(1,1'-biphenyl-4-ylsulfonyl)(4-benzyloxybenzyloxy)amino]acetate

Base Information

Chemical Name:tert-butyl [(1,1'-biphenyl-4-ylsulfonyl)(4-benzyloxybenzyloxy)amino]acetate
CAS No.:704889-03-2
Molecular Formula:C₃₂H₃₃NO₆S
Molecular Weight:559.683
Hs Code.:

Synonyms:tert-butyl [(1,1'-biphenyl-4-ylsulfonyl)(4-benzyloxybenzyloxy)amino]acetate

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Chemical Property of tert-butyl [(1,1'-biphenyl-4-ylsulfonyl)(4-benzyloxybenzyloxy)amino]acetate

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Technology Process of tert-butyl [(1,1'-biphenyl-4-ylsulfonyl)(4-benzyloxybenzyloxy)amino]acetate

There total 3 articles about tert-butyl [(1,1'-biphenyl-4-ylsulfonyl)(4-benzyloxybenzyloxy)amino]acetate 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: 60.0%

: 5292-43-3
bromoacetic acid tert-butyl ester

: 704888-97-1
N-(4-benzyloxy-benzyloxy)-1,1'-biphenyl-4-sulfonamide

: 704889-03-2
tert-butyl [(1,1'-biphenyl-4-ylsulfonyl)(4-benzyloxybenzyloxy)amino]acetate

Guidance literature:: With tetra(n-butyl)ammonium hydrogensulfate; caesium carbonate; In N,N-dimethyl-formamide; at 20 ℃; for 72h;
DOI:10.1016/j.bmc.2004.01.047

Reference yield:

: 1623-93-4
4-diphenylsulfonyl chloride

: 704889-03-2
tert-butyl [(1,1'-biphenyl-4-ylsulfonyl)(4-benzyloxybenzyloxy)amino]acetate

Guidance literature:: Multi-step reaction with 2 steps

1: 68 percent / N-methylmorpholine / tetrahydrofuran / 96 h / 20 °C

2: 60 percent / caesium carbonate; tetrabutylammonium hydrogensulfate / dimethylformamide / 72 h / 20 °C

With 4-methyl-morpholine; tetra(n-butyl)ammonium hydrogensulfate; caesium carbonate; In tetrahydrofuran; N,N-dimethyl-formamide;
DOI:10.1016/j.bmc.2004.01.047

Reference yield:

: O-(4-benzyloxy-benzyl)hydroxylamine hydrochloride

: 704889-03-2
tert-butyl [(1,1'-biphenyl-4-ylsulfonyl)(4-benzyloxybenzyloxy)amino]acetate

Guidance literature:: Multi-step reaction with 2 steps

1: 68 percent / N-methylmorpholine / tetrahydrofuran / 96 h / 20 °C

2: 60 percent / caesium carbonate; tetrabutylammonium hydrogensulfate / dimethylformamide / 72 h / 20 °C

With 4-methyl-morpholine; tetra(n-butyl)ammonium hydrogensulfate; caesium carbonate; In tetrahydrofuran; N,N-dimethyl-formamide;
DOI:10.1016/j.bmc.2004.01.047