{(3S,4R)-3-[(R)-1-(4-Nitro-benzyloxycarbonyloxy)-ethyl]-2-oxo-4-phenylsulfanylcarbonylmethyl-azetidin-1-yl}-oxo-acetic acid 4-nitro-benzyl ester

Base Information

Chemical Name:{(3S,4R)-3-[(R)-1-(4-Nitro-benzyloxycarbonyloxy)-ethyl]-2-oxo-4-phenylsulfanylcarbonylmethyl-azetidin-1-yl}-oxo-acetic acid 4-nitro-benzyl ester
CAS No.:90629-11-1
Molecular Formula:C₃₀H₂₅N₃O₁₂S
Molecular Weight:651.607
Hs Code.:

{(3S,4R)-3-[(R)-1-(4-Nitro-benzyloxycarbonyloxy)-ethyl]-2-oxo-4-phenylsulfanylcarbonylmethyl-azetidin-1-yl}-oxo-acetic acid 4-nitro-benzyl ester

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Chemical Property of {(3S,4R)-3-[(R)-1-(4-Nitro-benzyloxycarbonyloxy)-ethyl]-2-oxo-4-phenylsulfanylcarbonylmethyl-azetidin-1-yl}-oxo-acetic acid 4-nitro-benzyl ester

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Technology Process of {(3S,4R)-3-[(R)-1-(4-Nitro-benzyloxycarbonyloxy)-ethyl]-2-oxo-4-phenylsulfanylcarbonylmethyl-azetidin-1-yl}-oxo-acetic acid 4-nitro-benzyl ester

There total 5 articles about {(3S,4R)-3-[(R)-1-(4-Nitro-benzyloxycarbonyloxy)-ethyl]-2-oxo-4-phenylsulfanylcarbonylmethyl-azetidin-1-yl}-oxo-acetic acid 4-nitro-benzyl ester 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:

: 76899-07-5,78963-47-0,78963-48-1,78963-60-7,80951-41-3,81275-02-7,85647-75-2,85954-95-6,92217-74-8,104527-11-9,76855-69-1
(3R,4R)-3-[(R)-1-(tert-butyldimethylsilyloxy)ethyl]-4-acetoxyazetidin-2-one

: 90629-11-1
{(3S,4R)-3-[(R)-1-(4-Nitro-benzyloxycarbonyloxy)-ethyl]-2-oxo-4-phenylsulfanylcarbonylmethyl-azetidin-1-yl}-oxo-acetic acid 4-nitro-benzyl ester

Guidance literature:: Multi-step reaction with 5 steps

1: 100 percent / Et₃N / tetrahydrofuran / 2 h / Ambient temperature

2: 1) trimethylsilyl trifluoromethanesulfonate

3: boron trifluoride etherate / acetonitrile / 0.5 h / 0 °C

4: 45 percent / DMAP / CH₂Cl₂

5: Et₃N / CH₂Cl₂ / 0 °C

With dmap; boron trifluoride diethyl etherate; triethylamine; trimethylsilyl trifluoromethanesulfonate; In tetrahydrofuran; dichloromethane; acetonitrile;
DOI:10.1016/S0040-4039(01)81292-2

Reference yield:

: 86978-81-6
(3R,4R)-4-acetoxy-3-[(R)-1-(t-butyldimethylsilyloxy)ethyl]-1-trimethylsilyl-2-azetidinone

: 90629-11-1
{(3S,4R)-3-[(R)-1-(4-Nitro-benzyloxycarbonyloxy)-ethyl]-2-oxo-4-phenylsulfanylcarbonylmethyl-azetidin-1-yl}-oxo-acetic acid 4-nitro-benzyl ester

Guidance literature:: Multi-step reaction with 4 steps

1: 1) trimethylsilyl trifluoromethanesulfonate

2: boron trifluoride etherate / acetonitrile / 0.5 h / 0 °C

3: 45 percent / DMAP / CH₂Cl₂

4: Et₃N / CH₂Cl₂ / 0 °C

With dmap; boron trifluoride diethyl etherate; triethylamine; trimethylsilyl trifluoromethanesulfonate; In dichloromethane; acetonitrile;
DOI:10.1016/S0040-4039(01)81292-2