1-(tert-butyldimethylsilyl)-4-<3-hydroxy-4-nitro-4-(phenylthio)butyl>-2-azetidinone

Base Information

Chemical Name:1-(tert-butyldimethylsilyl)-4-<3-hydroxy-4-nitro-4-(phenylthio)butyl>-2-azetidinone
CAS No.:109996-05-6
Molecular Formula:C₁₉H₃₀N₂O₄SSi
Molecular Weight:410.61
Hs Code.:

Synonyms:1-(tert-butyldimethylsilyl)-4-<3-hydroxy-4-nitro-4-(phenylthio)butyl>-2-azetidinone

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Business phase:: The product has achieved commercial mass production^*data from LookChem market partment

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Chemical Property of 1-(tert-butyldimethylsilyl)-4-<3-hydroxy-4-nitro-4-(phenylthio)butyl>-2-azetidinone

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Technology Process of 1-(tert-butyldimethylsilyl)-4-<3-hydroxy-4-nitro-4-(phenylthio)butyl>-2-azetidinone

There total 5 articles about 1-(tert-butyldimethylsilyl)-4-<3-hydroxy-4-nitro-4-(phenylthio)butyl>-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:

: 74373-13-0
4-(but-3-en-1-yl)azetidin-2-one

: 109996-05-6
1-(tert-butyldimethylsilyl)-4-<3-hydroxy-4-nitro-4-(phenylthio)butyl>-2-azetidinone

Guidance literature:: Multi-step reaction with 3 steps

1: 100 percent / ethyldiisopropylamine / CH₂Cl₂ / 12 h / Ambient temperature

2: 1.) O₃, 2.) Me₂S / 1.) CH₂Cl₂, -78 deg C, 2.) CH₂Cl₂, reflux, 12 h

3: 1.) t-BuOK / 1.) THF, t-BuOH, 0 deg C, 2.) THF, t-BuOH, 0 deg C, 5 h

With dimethylsulfide; potassium tert-butylate; ozone; N-ethyl-N,N-diisopropylamine; In dichloromethane;
DOI:10.1021/jo00230a008

Reference yield:

: 18162-48-6
tert-butyldimethylsilyl chloride

: 109996-05-6
1-(tert-butyldimethylsilyl)-4-<3-hydroxy-4-nitro-4-(phenylthio)butyl>-2-azetidinone

Guidance literature:: Multi-step reaction with 3 steps

1: 100 percent / ethyldiisopropylamine / CH₂Cl₂ / 12 h / Ambient temperature

2: 1.) O₃, 2.) Me₂S / 1.) CH₂Cl₂, -78 deg C, 2.) CH₂Cl₂, reflux, 12 h

3: 1.) t-BuOK / 1.) THF, t-BuOH, 0 deg C, 2.) THF, t-BuOH, 0 deg C, 5 h

With dimethylsulfide; potassium tert-butylate; ozone; N-ethyl-N,N-diisopropylamine; In dichloromethane;
DOI:10.1021/jo00230a008

Reference yield:

: 931-59-9
benzenesulfenyl chloride

: 109996-05-6
1-(tert-butyldimethylsilyl)-4-<3-hydroxy-4-nitro-4-(phenylthio)butyl>-2-azetidinone

Guidance literature:: Multi-step reaction with 2 steps

1: 46 percent / tetrahydrofuran; ethanol

2: 1.) t-BuOK / 1.) THF, t-BuOH, 0 deg C, 2.) THF, t-BuOH, 0 deg C, 5 h

With potassium tert-butylate; In tetrahydrofuran; ethanol;
DOI:10.1021/jo00230a008