((R)-2-Benzenesulfonyl-1-benzyloxymethyl-ethyl)-benzyl-(S)-1-oxiranylmethyl-amine

Base Information

Chemical Name:((R)-2-Benzenesulfonyl-1-benzyloxymethyl-ethyl)-benzyl-(S)-1-oxiranylmethyl-amine
CAS No.:212266-71-2
Molecular Formula:C₂₆H₂₉NO₄S
Molecular Weight:451.587
Hs Code.:

Synonyms:((R)-2-Benzenesulfonyl-1-benzyloxymethyl-ethyl)-benzyl-(S)-1-oxiranylmethyl-amine

Suppliers and Price of ((R)-2-Benzenesulfonyl-1-benzyloxymethyl-ethyl)-benzyl-(S)-1-oxiranylmethyl-amine

Supply Marketing:

Business phase:: The product has achieved commercial mass production^*data from LookChem market partment

Manufacturers and distributors:

Manufacture/Brand
Chemicals and raw materials
Packaging
price

Total 0 raw suppliers

Chemical Property of ((R)-2-Benzenesulfonyl-1-benzyloxymethyl-ethyl)-benzyl-(S)-1-oxiranylmethyl-amine

Chemical Property:

Purity/Quality:

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:

Useful:

Technology Process of ((R)-2-Benzenesulfonyl-1-benzyloxymethyl-ethyl)-benzyl-(S)-1-oxiranylmethyl-amine

There total 4 articles about ((R)-2-Benzenesulfonyl-1-benzyloxymethyl-ethyl)-benzyl-(S)-1-oxiranylmethyl-amine 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: 99.0%

: 212266-70-1
Toluene-4-sulfonic acid (S)-3-[((R)-2-benzenesulfonyl-1-benzyloxymethyl-ethyl)-benzyl-amino]-2-hydroxy-propyl ester

: 212266-71-2
((R)-2-Benzenesulfonyl-1-benzyloxymethyl-ethyl)-benzyl-(S)-1-oxiranylmethyl-amine

Guidance literature:: With potassium carbonate; In water; N,N-dimethyl-formamide; for 24h; Ambient temperature;
DOI:10.1016/S0040-4039(98)01171-X

Reference yield:

: 100-39-0
benzyl bromide

: 212266-71-2
((R)-2-Benzenesulfonyl-1-benzyloxymethyl-ethyl)-benzyl-(S)-1-oxiranylmethyl-amine

Guidance literature:: Multi-step reaction with 6 steps

1: 86 percent / 1.) NaH, 2.) n-Bu₄NI / tetrahydrofuran / 24 h / 0 °C

2: 95 percent / 3M HCl / ethyl acetate / 1 h / Ambient temperature

3: 97 percent / NaBH(OAc)3 / 1,2-dichloro-ethane / Ambient temperature

4: 94 percent / 4M HCl / tetrahydrofuran / 3 h / Ambient temperature

5: 85 percent / pyridine / 24 h / 0 °C

6: 99 percent / K₂CO₃ / H₂O; dimethylformamide / 24 h / Ambient temperature

With pyridine; hydrogenchloride; tetra-(n-butyl)ammonium iodide; sodium tris(acetoxy)borohydride; sodium hydride; potassium carbonate; In tetrahydrofuran; water; ethyl acetate; 1,2-dichloro-ethane; N,N-dimethyl-formamide;
DOI:10.1016/S0040-4039(98)01171-X

Reference yield:

: 116611-44-0
((R)-2-benzenesulfonyl-1-hydroxymethyl-ethyl)carbamic acid tert-butyl ester

: 212266-71-2
((R)-2-Benzenesulfonyl-1-benzyloxymethyl-ethyl)-benzyl-(S)-1-oxiranylmethyl-amine

Guidance literature:: Multi-step reaction with 6 steps

1: 86 percent / 1.) NaH, 2.) n-Bu₄NI / tetrahydrofuran / 24 h / 0 °C

2: 95 percent / 3M HCl / ethyl acetate / 1 h / Ambient temperature

3: 97 percent / NaBH(OAc)3 / 1,2-dichloro-ethane / Ambient temperature

4: 94 percent / 4M HCl / tetrahydrofuran / 3 h / Ambient temperature

5: 85 percent / pyridine / 24 h / 0 °C

6: 99 percent / K₂CO₃ / H₂O; dimethylformamide / 24 h / Ambient temperature

With pyridine; hydrogenchloride; tetra-(n-butyl)ammonium iodide; sodium tris(acetoxy)borohydride; sodium hydride; potassium carbonate; In tetrahydrofuran; water; ethyl acetate; 1,2-dichloro-ethane; N,N-dimethyl-formamide;
DOI:10.1016/S0040-4039(98)01171-X