benzyl (3R,4R,5S)-3-hydroxy-4-(4-hydroxyphenyl)-5-triisopropylsilanyloxymethyl-piperidine-1-carboxylate

Base Information

Chemical Name:benzyl (3R,4R,5S)-3-hydroxy-4-(4-hydroxyphenyl)-5-triisopropylsilanyloxymethyl-piperidine-1-carboxylate
CAS No.:912347-08-1
Molecular Formula:C₂₉H₄₃NO₅Si
Molecular Weight:513.75
Hs Code.:

Synonyms:benzyl (3R,4R,5S)-3-hydroxy-4-(4-hydroxyphenyl)-5-triisopropylsilanyloxymethyl-piperidine-1-carboxylate

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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 benzyl (3R,4R,5S)-3-hydroxy-4-(4-hydroxyphenyl)-5-triisopropylsilanyloxymethyl-piperidine-1-carboxylate

Chemical Property:

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Technology Process of benzyl (3R,4R,5S)-3-hydroxy-4-(4-hydroxyphenyl)-5-triisopropylsilanyloxymethyl-piperidine-1-carboxylate

There total 2 articles about benzyl (3R,4R,5S)-3-hydroxy-4-(4-hydroxyphenyl)-5-triisopropylsilanyloxymethyl-piperidine-1-carboxylate 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:

: 303043-56-3
benzyl (3R,4R,5S)-3-hydroxy-5-hydroxymethyl-4-(4-hydroxyphenyl)piperidine-1-carboxylate

: 13154-24-0
triisopropylsilyl chloride

: 912347-08-1
benzyl (3R,4R,5S)-3-hydroxy-4-(4-hydroxyphenyl)-5-triisopropylsilanyloxymethyl-piperidine-1-carboxylate

Guidance literature:: With 1H-imidazole; In N,N-dimethyl-formamide; at 20 ℃; for 16h;

Reference yield:

: 303043-56-3
(3R,4R,5S)-5-hydroxymethyl-4-(4-hydroxy-phenyl)-piperidin-3-ol hydrobromide

: 501-53-1,94274-21-2
benzyl chloroformate

: 912347-08-1
benzyl (3R,4R,5S)-3-hydroxy-4-(4-hydroxyphenyl)-5-triisopropylsilanyloxymethyl-piperidine-1-carboxylate

Guidance literature:: Multi-step reaction with 2 steps

1: sodium carbonate / ethyl acetate / 5 h / 0 °C

2: 1H-imidazole / N,N-dimethyl-formamide / 16 h / 20 °C

With 1H-imidazole; sodium carbonate; In ethyl acetate; N,N-dimethyl-formamide;