3,3-diethyl-4-<<4-<(1,1-dimethylethoxy)carbonyl>phenyl>oxy>-1-(N-benzyl-N-ethylcarbamoyl)-2-azetidinone

Base Information

Chemical Name:3,3-diethyl-4-<<4-<(1,1-dimethylethoxy)carbonyl>phenyl>oxy>-1-(N-benzyl-N-ethylcarbamoyl)-2-azetidinone
CAS No.:143818-79-5
Molecular Formula:C₂₈H₃₆N₂O₅
Molecular Weight:480.604
Hs Code.:

Synonyms:3,3-diethyl-4-<<4-<(1,1-dimethylethoxy)carbonyl>phenyl>oxy>-1-(N-benzyl-N-ethylcarbamoyl)-2-azetidinone

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Chemical Property of 3,3-diethyl-4-<<4-<(1,1-dimethylethoxy)carbonyl>phenyl>oxy>-1-(N-benzyl-N-ethylcarbamoyl)-2-azetidinone

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Technology Process of 3,3-diethyl-4-<<4-<(1,1-dimethylethoxy)carbonyl>phenyl>oxy>-1-(N-benzyl-N-ethylcarbamoyl)-2-azetidinone

There total 5 articles about 3,3-diethyl-4-<<4-<(1,1-dimethylethoxy)carbonyl>phenyl>oxy>-1-(N-benzyl-N-ethylcarbamoyl)-2-azetidinone 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:

: 97-96-1
2-Ethylbutyraldehyde

: 143818-79-5
3,3-diethyl-4-<<4-<(1,1-dimethylethoxy)carbonyl>phenyl>oxy>-1-(N-benzyl-N-ethylcarbamoyl)-2-azetidinone

Guidance literature:: Multi-step reaction with 4 steps

1: 55 percent / sodium acetate / 48 h / Heating

2: 36 percent / CH₂Cl₂ / Ambient temperature

3: 85 percent / acetone / 0.5 h

4: triethylamine, 4-(dimethylamino)pyridine / CH₂Cl₂ / 16 h / Heating

With dmap; sodium acetate; triethylamine; In dichloromethane; acetone;
DOI:10.1021/jm00099a003

Reference yield:

: 22014-15-9
1-acetoxy-2-ethyl-1-butene

: 143818-79-5
3,3-diethyl-4-<<4-<(1,1-dimethylethoxy)carbonyl>phenyl>oxy>-1-(N-benzyl-N-ethylcarbamoyl)-2-azetidinone

Guidance literature:: Multi-step reaction with 3 steps

1: 36 percent / CH₂Cl₂ / Ambient temperature

2: 85 percent / acetone / 0.5 h

3: triethylamine, 4-(dimethylamino)pyridine / CH₂Cl₂ / 16 h / Heating

With dmap; triethylamine; In dichloromethane; acetone;
DOI:10.1021/jm00099a003

Reference yield:

: 14321-27-8
N-ethylbenzylamine

: 143818-79-5
3,3-diethyl-4-<<4-<(1,1-dimethylethoxy)carbonyl>phenyl>oxy>-1-(N-benzyl-N-ethylcarbamoyl)-2-azetidinone

Guidance literature:: Multi-step reaction with 2 steps

1: ethyl acetate / Heating

2: triethylamine, 4-(dimethylamino)pyridine / CH₂Cl₂ / 16 h / Heating

With dmap; triethylamine; In dichloromethane; ethyl acetate;
DOI:10.1021/jm00099a003