(3S,4S)-3-Benzyloxy-1-[bis-(4-methoxy-phenyl)-methyl]-4-[(R)-(tert-butyl-dimethyl-silanyloxy)-phenyl-methyl]-azetidin-2-one

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Chemical Name:(3S,4S)-3-Benzyloxy-1-[bis-(4-methoxy-phenyl)-methyl]-4-[(R)-(tert-butyl-dimethyl-silanyloxy)-phenyl-methyl]-azetidin-2-one
CAS No.:130193-85-0
Molecular Formula:C₃₈H₄₅NO₅Si
Molecular Weight:623.864
Hs Code.:

Synonyms:(3S,4S)-3-Benzyloxy-1-[bis-(4-methoxy-phenyl)-methyl]-4-[(R)-(tert-butyl-dimethyl-silanyloxy)-phenyl-methyl]-azetidin-2-one

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Chemical Property of (3S,4S)-3-Benzyloxy-1-[bis-(4-methoxy-phenyl)-methyl]-4-[(R)-(tert-butyl-dimethyl-silanyloxy)-phenyl-methyl]-azetidin-2-one

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Technology Process of (3S,4S)-3-Benzyloxy-1-[bis-(4-methoxy-phenyl)-methyl]-4-[(R)-(tert-butyl-dimethyl-silanyloxy)-phenyl-methyl]-azetidin-2-one

There total 6 articles about (3S,4S)-3-Benzyloxy-1-[bis-(4-methoxy-phenyl)-methyl]-4-[(R)-(tert-butyl-dimethyl-silanyloxy)-phenyl-methyl]-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:

: 19293-62-0
p,p'-dimethoxybenzhydrylamine

: 130193-85-0
(3S,4S)-3-Benzyloxy-1-[bis-(4-methoxy-phenyl)-methyl]-4-[(R)-(tert-butyl-dimethyl-silanyloxy)-phenyl-methyl]-azetidin-2-one

Guidance literature:: Multi-step reaction with 2 steps

1: MgSO₄ / toluene / 1 h / 0 °C

2: Et₃N / CH₂Cl₂ / Ambient temperature

With magnesium sulfate; triethylamine; In dichloromethane; toluene;
DOI:10.1016/S0040-4020(01)88510-0

Reference yield:

: 20698-91-3
(R)-methyl mandelate

: 130193-85-0
(3S,4S)-3-Benzyloxy-1-[bis-(4-methoxy-phenyl)-methyl]-4-[(R)-(tert-butyl-dimethyl-silanyloxy)-phenyl-methyl]-azetidin-2-one

Guidance literature:: Multi-step reaction with 4 steps

1: 98 percent / imidazole / dimethylformamide / Ambient temperature

2: 82 percent / DIBAL / hexane; diethyl ether / 0.33 h / -78 °C

3: MgSO₄ / toluene / 1 h / 0 °C

4: Et₃N / CH₂Cl₂ / Ambient temperature

With 1H-imidazole; diisobutylaluminium hydride; magnesium sulfate; triethylamine; In diethyl ether; hexane; dichloromethane; N,N-dimethyl-formamide; toluene;
DOI:10.1016/S0040-4020(01)88510-0

Reference yield:

: 124876-74-0
Methyl (R)-(-)-α-<<(1,1-dimethylethyl)dimethylsilyl>oxy>-α-phenylacetate

: 130193-85-0
(3S,4S)-3-Benzyloxy-1-[bis-(4-methoxy-phenyl)-methyl]-4-[(R)-(tert-butyl-dimethyl-silanyloxy)-phenyl-methyl]-azetidin-2-one

Guidance literature:: Multi-step reaction with 3 steps

1: 82 percent / DIBAL / hexane; diethyl ether / 0.33 h / -78 °C

2: MgSO₄ / toluene / 1 h / 0 °C

3: Et₃N / CH₂Cl₂ / Ambient temperature

With diisobutylaluminium hydride; magnesium sulfate; triethylamine; In diethyl ether; hexane; dichloromethane; toluene;
DOI:10.1016/S0040-4020(01)88510-0