N-Nenzoyl-2-<3',4'-bis<(tert-butyldimethylsilyl)oxy>benzyl>homoserine lactone

Base Information

Chemical Name:N-Nenzoyl-2-<3',4'-bis<(tert-butyldimethylsilyl)oxy>benzyl>homoserine lactone
CAS No.:152774-31-7
Molecular Formula:C₃₀H₄₅NO₅Si₂
Molecular Weight:555.862
Hs Code.:

Synonyms:N-Nenzoyl-2-<3',4'-bis<(tert-butyldimethylsilyl)oxy>benzyl>homoserine lactone

Suppliers and Price of N-Nenzoyl-2-<3',4'-bis<(tert-butyldimethylsilyl)oxy>benzyl>homoserine lactone

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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 N-Nenzoyl-2-<3',4'-bis<(tert-butyldimethylsilyl)oxy>benzyl>homoserine lactone

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Technology Process of N-Nenzoyl-2-<3',4'-bis<(tert-butyldimethylsilyl)oxy>benzyl>homoserine lactone

There total 5 articles about N-Nenzoyl-2-<3',4'-bis<(tert-butyldimethylsilyl)oxy>benzyl>homoserine lactone 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: 84.0%

: 75-21-8,99932-75-9
oxirane

: 152774-26-0
Methyl N-benzoyl-3',4'bis<(tert-butyldimethylsilyl)oxy>phenylalaninate

: 152774-31-7
N-Nenzoyl-2-<3',4'-bis<(tert-butyldimethylsilyl)oxy>benzyl>homoserine lactone

Guidance literature:: With lithium diisopropyl amide; In tetrahydrofuran; at -78 ℃;

Reference yield:

: 54210-15-0
N-benzoyl-3,4-dihydroxyphenylalanine methyl ester

: 152774-31-7
N-Nenzoyl-2-<3',4'-bis<(tert-butyldimethylsilyl)oxy>benzyl>homoserine lactone

Guidance literature:: Multi-step reaction with 2 steps

1: 74 percent / imidazole, 4-(dimethylamino)pyridine / 3 h / 50 °C

2: 84 percent / LDA / tetrahydrofuran / -78 °C

With 1H-imidazole; dmap; lithium diisopropyl amide; In tetrahydrofuran;

Reference yield:

: 98-88-4
benzoyl chloride

: 152774-31-7
N-Nenzoyl-2-<3',4'-bis<(tert-butyldimethylsilyl)oxy>benzyl>homoserine lactone

Guidance literature:: Multi-step reaction with 4 steps

1: 88 percent / 4-(dimethylamino)pyridine / pyridine / 1 h / Ambient temperature

2: 81 percent / K₂CO₃ / methanol; tetrahydrofuran / 2 h / Ambient temperature

3: 74 percent / imidazole, 4-(dimethylamino)pyridine / 3 h / 50 °C

4: 84 percent / LDA / tetrahydrofuran / -78 °C

With 1H-imidazole; dmap; potassium carbonate; lithium diisopropyl amide; In tetrahydrofuran; pyridine; methanol;