{3-[(2S,3R)-3-((S)-1-Hydroxy-ethyl)-4-oxo-azetidin-2-yl]-2-oxo-propyl}-phosphonic acid benzyl ester methyl ester

Base Information

Chemical Name:{3-[(2S,3R)-3-((S)-1-Hydroxy-ethyl)-4-oxo-azetidin-2-yl]-2-oxo-propyl}-phosphonic acid benzyl ester methyl ester
CAS No.:86509-41-3
Molecular Formula:C₁₆H₂₂NO₆P
Molecular Weight:355.328
Hs Code.:

Synonyms:{3-[(2S,3R)-3-((S)-1-Hydroxy-ethyl)-4-oxo-azetidin-2-yl]-2-oxo-propyl}-phosphonic acid benzyl ester methyl ester

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Chemical Property of {3-[(2S,3R)-3-((S)-1-Hydroxy-ethyl)-4-oxo-azetidin-2-yl]-2-oxo-propyl}-phosphonic acid benzyl ester methyl ester

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Technology Process of {3-[(2S,3R)-3-((S)-1-Hydroxy-ethyl)-4-oxo-azetidin-2-yl]-2-oxo-propyl}-phosphonic acid benzyl ester methyl ester

There total 9 articles about {3-[(2S,3R)-3-((S)-1-Hydroxy-ethyl)-4-oxo-azetidin-2-yl]-2-oxo-propyl}-phosphonic acid benzyl ester methyl 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: 57.0%

: 86509-39-9
(3-{(2S,3R)-3-[(S)-1-(tert-Butyl-dimethyl-silanyloxy)-ethyl]-4-oxo-azetidin-2-yl}-2-oxo-propyl)-phosphonic acid benzyl ester methyl ester

: 86509-41-3
{3-[(2S,3R)-3-((S)-1-Hydroxy-ethyl)-4-oxo-azetidin-2-yl]-2-oxo-propyl}-phosphonic acid benzyl ester methyl ester

Guidance literature:: With hydrogenchloride; In methanol; at 0 ℃; for 4h;
DOI:10.1016/S0040-4039(00)81403-3

Reference yield:

: 19236-58-9
dibenzyl methylphosphonate

: 86509-41-3
{3-[(2S,3R)-3-((S)-1-Hydroxy-ethyl)-4-oxo-azetidin-2-yl]-2-oxo-propyl}-phosphonic acid benzyl ester methyl ester

Guidance literature:: Multi-step reaction with 5 steps

1: 1N NaOH / tetrahydrofuran / 48 h

3: 45 percent / nBuLi / tetrahydrofuran / -78 - 25 °C

4: 80 percent / tetrabutylammonium fluoride / CH₂Cl₂ / -78 °C

5: 57 percent / HCl / methanol / 4 h / 0 °C

With hydrogenchloride; sodium hydroxide; n-butyllithium; tetrabutyl ammonium fluoride; In tetrahydrofuran; methanol; dichloromethane;
DOI:10.1016/S0040-4039(00)81403-3

Reference yield:

: 538-60-3
dibenzyl hydrogen phosphite

: 86509-41-3
{3-[(2S,3R)-3-((S)-1-Hydroxy-ethyl)-4-oxo-azetidin-2-yl]-2-oxo-propyl}-phosphonic acid benzyl ester methyl ester

Guidance literature:: Multi-step reaction with 6 steps

1: NaH / dimethylformamide / 0 °C

2: 1N NaOH / tetrahydrofuran / 48 h

4: 45 percent / nBuLi / tetrahydrofuran / -78 - 25 °C

5: 80 percent / tetrabutylammonium fluoride / CH₂Cl₂ / -78 °C

6: 57 percent / HCl / methanol / 4 h / 0 °C

With hydrogenchloride; sodium hydroxide; n-butyllithium; tetrabutyl ammonium fluoride; sodium hydride; In tetrahydrofuran; methanol; dichloromethane; N,N-dimethyl-formamide;
DOI:10.1016/S0040-4039(00)81403-3