1-(tert-butyldimethylsilyl)-4-<5-nitro-5-(phenylthio)-4-(Z)-pentenyl>-2-azetidinone

Base Information

Chemical Name:1-(tert-butyldimethylsilyl)-4-<5-nitro-5-(phenylthio)-4-(Z)-pentenyl>-2-azetidinone
CAS No.:109975-74-8
Molecular Formula:C₂₀H₃₀N₂O₃SSi
Molecular Weight:406.621
Hs Code.:

Synonyms:1-(tert-butyldimethylsilyl)-4-<5-nitro-5-(phenylthio)-4-(Z)-pentenyl>-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-<5-nitro-5-(phenylthio)-4-(Z)-pentenyl>-2-azetidinone

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Technology Process of 1-(tert-butyldimethylsilyl)-4-<5-nitro-5-(phenylthio)-4-(Z)-pentenyl>-2-azetidinone

There total 10 articles about 1-(tert-butyldimethylsilyl)-4-<5-nitro-5-(phenylthio)-4-(Z)-pentenyl>-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: 81.0%

: 109975-73-7
1-(tert-butyldimethylsilyl)-4-<4-hydroxy-5-nitro-5-(phenylthio)pentyl>-2-azetidinone

: 109975-74-8
1-(tert-butyldimethylsilyl)-4-<5-nitro-5-(phenylthio)-4-(Z)-pentenyl>-2-azetidinone

Guidance literature:: With methanesulfonyl chloride; triethylamine; In dichloromethane; 1.) -78 deg C, 5 min, 2.) 0 deg C, 20 min;
DOI:10.1021/jo00230a008

Reference yield:

: 96746-26-8
4-(4-pentenyl)-2-azetidinone

: 109975-74-8
1-(tert-butyldimethylsilyl)-4-<5-nitro-5-(phenylthio)-4-(Z)-pentenyl>-2-azetidinone

Guidance literature:: Multi-step reaction with 2 steps

1: 1.) i-Pr₂NEt, 2.) O₃, Me₂S / 1.) CH₂Cl₂, 25 deg C, 2.) -78 deg C

2: 1.) t-BuOH, t-BuOK, 2.)Et₃N, MeSO₂Cl / 1.) THF, 0 deg C, 2.) -78 deg C to 0 deg C

With dimethylsulfide; potassium tert-butylate; ozone; methanesulfonyl chloride; triethylamine; N-ethyl-N,N-diisopropylamine; tert-butyl alcohol;
DOI:10.1021/jo00214a049

Reference yield:

: 3070-53-9
1,6-heptadiene

: 109975-74-8
1-(tert-butyldimethylsilyl)-4-<5-nitro-5-(phenylthio)-4-(Z)-pentenyl>-2-azetidinone

Guidance literature:: Multi-step reaction with 6 steps

1: 24 h / Ambient temperature

2: aq. sodium sulfite, aq. KOH / CH₂Cl₂

3: 99 percent / ethyldiisopropylamine / CH₂Cl₂ / 12 h / Ambient temperature

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

5: 1.) KO-t-Bu / 1.) THF, t-BuOH, 0 deg C, 20 min, 2.) THF, t-BuOH, -3 deg C to 0 deg C, 18 h

6: 81 percent / MeSO₂Cl, Et₃N / CH₂Cl₂ / 1.) -78 deg C, 5 min, 2.) 0 deg C, 20 min

With potassium hydroxide; dimethylsulfide; potassium tert-butylate; ozone; methanesulfonyl chloride; triethylamine; N-ethyl-N,N-diisopropylamine; sodium sulfite; In dichloromethane;
DOI:10.1021/jo00230a008