tert-butyl (2R,3S,4R,5S)-3-(benzyloxy)-4,5-dihydroxy-2-(2-hydroxyethyl)piperidine-1-carboxylate

Base Information

Chemical Name:tert-butyl (2R,3S,4R,5S)-3-(benzyloxy)-4,5-dihydroxy-2-(2-hydroxyethyl)piperidine-1-carboxylate
CAS No.:915307-19-6
Molecular Formula:C₁₉H₂₉NO₆
Molecular Weight:367.442
Hs Code.:

Synonyms:tert-butyl (2R,3S,4R,5S)-3-(benzyloxy)-4,5-dihydroxy-2-(2-hydroxyethyl)piperidine-1-carboxylate

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Chemical Property of tert-butyl (2R,3S,4R,5S)-3-(benzyloxy)-4,5-dihydroxy-2-(2-hydroxyethyl)piperidine-1-carboxylate

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Technology Process of tert-butyl (2R,3S,4R,5S)-3-(benzyloxy)-4,5-dihydroxy-2-(2-hydroxyethyl)piperidine-1-carboxylate

There total 1 articles about tert-butyl (2R,3S,4R,5S)-3-(benzyloxy)-4,5-dihydroxy-2-(2-hydroxyethyl)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: 92.0%

: (3S,4R,5S,6R)-5-(benzyloxy)-6-(2-hydroxyethyl)piperidine-3,4-diol hydrochloride

: 24424-99-5
di-tert-butyl dicarbonate

: 915307-19-6
tert-butyl (2R,3S,4R,5S)-3-(benzyloxy)-4,5-dihydroxy-2-(2-hydroxyethyl)piperidine-1-carboxylate

Guidance literature:: With triethylamine; In dichloromethane; at 20 ℃; for 8h;
DOI:10.1021/jo061455v

Reference yield:

: 915307-19-6
tert-butyl (2R,3S,4R,5S)-3-(benzyloxy)-4,5-dihydroxy-2-(2-hydroxyethyl)piperidine-1-carboxylate

: 915307-20-9
(4aR,5S,6R,7S)-5-(benzyloxy)-6,7-dihydroxyhexahydropyrido[1,2-c][1,3]oxazin-1-one

Guidance literature:: Multi-step reaction with 2 steps

1: triethylamine / CH₂Cl₂ / 0.17 h / 0 °C

2: 89 percent / K₂CO₃ / acetonitrile / 6 h / Heating

With potassium carbonate; triethylamine; In dichloromethane; acetonitrile;
DOI:10.1021/jo061455v