(3R,4R)-1-(benzyloxycarbonyl-1-triphenylphosphoranylidenemethyl)-3-<(1R)-1-tert-butyldimethylsilyloxyethyl>-4-(3-acetoxy-2-oxopropane-1-oxy)azetidin-2-one

Base Information

Chemical Name:(3R,4R)-1-(benzyloxycarbonyl-1-triphenylphosphoranylidenemethyl)-3-<(1R)-1-tert-butyldimethylsilyloxyethyl>-4-(3-acetoxy-2-oxopropane-1-oxy)azetidin-2-one
CAS No.:129441-49-2
Molecular Formula:C₄₃H₅₀NO₈PSi
Molecular Weight:767.931
Hs Code.:

(3R,4R)-1-(benzyloxycarbonyl-1-triphenylphosphoranylidenemethyl)-3-<(1R)-1-tert-butyldimethylsilyloxyethyl>-4-(3-acetoxy-2-oxopropane-1-oxy)azetidin-2-one

Synonyms:(3R,4R)-1-(benzyloxycarbonyl-1-triphenylphosphoranylidenemethyl)-3-<(1R)-1-tert-butyldimethylsilyloxyethyl>-4-(3-acetoxy-2-oxopropane-1-oxy)azetidin-2-one

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Chemical Property of (3R,4R)-1-(benzyloxycarbonyl-1-triphenylphosphoranylidenemethyl)-3-<(1R)-1-tert-butyldimethylsilyloxyethyl>-4-(3-acetoxy-2-oxopropane-1-oxy)azetidin-2-one

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Technology Process of (3R,4R)-1-(benzyloxycarbonyl-1-triphenylphosphoranylidenemethyl)-3-<(1R)-1-tert-butyldimethylsilyloxyethyl>-4-(3-acetoxy-2-oxopropane-1-oxy)azetidin-2-one

There total 8 articles about (3R,4R)-1-(benzyloxycarbonyl-1-triphenylphosphoranylidenemethyl)-3-<(1R)-1-tert-butyldimethylsilyloxyethyl>-4-(3-acetoxy-2-oxopropane-1-oxy)azetidin-2-one 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

: 129441-49-2
(3R,4R)-1-(benzyloxycarbonyl-1-triphenylphosphoranylidenemethyl)-3-<(1R)-1-tert-butyldimethylsilyloxyethyl>-4-(3-acetoxy-2-oxopropane-1-oxy)azetidin-2-one

Guidance literature:: Multi-step reaction with 5 steps

1: 86 percent / zinc acetate / benzene / 8.5 h / Heating

2: 49 percent / 1.) oxalyl chloride, DMSO, 2.) Et₃N / CH₂Cl₂ / -50 °C / 1.) 15 min, 2.) 1 h

3: Et₃N / tetrahydrofuran / 3 h / Ambient temperature

4: 2,6-lutidine, thionyl chloride / CH₂Cl₂ / 0.75 h / -40 °C

5: CH₂Cl₂ / Ambient temperature

With 2,6-dimethylpyridine; thionyl chloride; oxalyl dichloride; zinc diacetate; dimethyl sulfoxide; triethylamine; In tetrahydrofuran; dichloromethane; benzene;

Reference yield:

: 93713-40-7
Glycerin-monoacetat

: 129441-49-2
(3R,4R)-1-(benzyloxycarbonyl-1-triphenylphosphoranylidenemethyl)-3-<(1R)-1-tert-butyldimethylsilyloxyethyl>-4-(3-acetoxy-2-oxopropane-1-oxy)azetidin-2-one

Guidance literature:: Multi-step reaction with 5 steps

1: 86 percent / zinc acetate / benzene / 8.5 h / Heating

2: 49 percent / 1.) oxalyl chloride, DMSO, 2.) Et₃N / CH₂Cl₂ / -50 °C / 1.) 15 min, 2.) 1 h

3: Et₃N / tetrahydrofuran / 3 h / Ambient temperature

4: 2,6-lutidine, thionyl chloride / CH₂Cl₂ / 0.75 h / -40 °C

5: CH₂Cl₂ / Ambient temperature

With 2,6-dimethylpyridine; thionyl chloride; oxalyl dichloride; zinc diacetate; dimethyl sulfoxide; triethylamine; In tetrahydrofuran; dichloromethane; benzene;

Reference yield:

: 123657-02-3
(3R,4R)-4-allyloxy-3-<(1R)-1-tert-butyldimethylsilyloxyethyl>azetidin-2-one

: 129441-49-2
(3R,4R)-1-(benzyloxycarbonyl-1-triphenylphosphoranylidenemethyl)-3-<(1R)-1-tert-butyldimethylsilyloxyethyl>-4-(3-acetoxy-2-oxopropane-1-oxy)azetidin-2-one

Guidance literature:: Multi-step reaction with 6 steps

1: 91 percent / 70percent m-chloroperbenzoic acid, NaHCO₃ / CH₂Cl₂ / Ambient temperature

2: 77 percent / Ti(iOPr)4 / 6 h / Ambient temperature

3: 49 percent / 1.) oxalyl chloride, DMSO, 2.) Et₃N / CH₂Cl₂ / -50 °C / 1.) 15 min, 2.) 1 h

4: Et₃N / tetrahydrofuran / 3 h / Ambient temperature

5: 2,6-lutidine, thionyl chloride / CH₂Cl₂ / 0.75 h / -40 °C

6: CH₂Cl₂ / Ambient temperature

With 2,6-dimethylpyridine; titanium(IV) isopropylate; thionyl chloride; oxalyl dichloride; sodium hydrogencarbonate; dimethyl sulfoxide; triethylamine; 3-chloro-benzenecarboperoxoic acid; In tetrahydrofuran; dichloromethane;