(4R)-N-benzyl-N-(tert-butyloxycarbonyl)-4-diphenylphosphatoxy-5-methyl-5-nitro-hexylamine

Base Information

Chemical Name:(4R)-N-benzyl-N-(tert-butyloxycarbonyl)-4-diphenylphosphatoxy-5-methyl-5-nitro-hexylamine
CAS No.:615268-20-7
Molecular Formula:C₃₁H₃₉N₂O₈P
Molecular Weight:598.633
Hs Code.:

Synonyms:(4R)-N-benzyl-N-(tert-butyloxycarbonyl)-4-diphenylphosphatoxy-5-methyl-5-nitro-hexylamine

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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 (4R)-N-benzyl-N-(tert-butyloxycarbonyl)-4-diphenylphosphatoxy-5-methyl-5-nitro-hexylamine

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Technology Process of (4R)-N-benzyl-N-(tert-butyloxycarbonyl)-4-diphenylphosphatoxy-5-methyl-5-nitro-hexylamine

There total 2 articles about (4R)-N-benzyl-N-(tert-butyloxycarbonyl)-4-diphenylphosphatoxy-5-methyl-5-nitro-hexylamine 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: 98.0%

: 2524-64-3
chlorophosphoric acid diphenyl ester

: 615268-18-3
(4R)-N-benzyl-N-(tert-butyloxycarbonyl)-4-hydroxy-5-methyl-5-nitro-hexylamine

: 615268-20-7
(4R)-N-benzyl-N-(tert-butyloxycarbonyl)-4-diphenylphosphatoxy-5-methyl-5-nitro-hexylamine

Guidance literature:: With dmap; In dichloromethane; at 20 ℃;
DOI:10.1021/ol035564x

Reference yield:

: 213772-31-7
4-[N-benzyl-N-(tert-butyloxycarbonyl)]-amino-1-butanal

: 615268-20-7
(4R)-N-benzyl-N-(tert-butyloxycarbonyl)-4-diphenylphosphatoxy-5-methyl-5-nitro-hexylamine

Guidance literature:: Multi-step reaction with 4 steps

1: 94 percent / potassium tert-butoxide / acetonitrile; 2-methyl-propan-2-ol

2: 88 percent / oxalyl chloride; DMSO; triethylamine / CH₂Cl₂ / 1.33 h / cooling

3: (S)-(-)-α,α-diphenyl-2-pyrrolidinemethanol; borane dimethyl sulfide complex / tetrahydrofuran / 0.83 h / Heating

4: DMAP / CH₂Cl₂ / 20 °C

With dmap; oxalyl dichloride; (S)-diphenylprolinol; dimethylsulfide borane complex; potassium tert-butylate; dimethyl sulfoxide; triethylamine; In tetrahydrofuran; dichloromethane; acetonitrile; tert-butyl alcohol; 1: Henry reaction / 2: Swern oxidation;
DOI:10.1016/j.tet.2006.03.063