(3S,4R,5R,6R)-4,5-bis(benzyloxy)-6-(3'-hydroxy-(S)-1'-hydroxypropyl)-piperidin-3-yl pivalate

Base Information

Chemical Name:(3S,4R,5R,6R)-4,5-bis(benzyloxy)-6-(3'-hydroxy-(S)-1'-hydroxypropyl)-piperidin-3-yl pivalate
CAS No.:1255955-57-7
Molecular Formula:C₂₇H₃₇NO₆
Molecular Weight:471.594
Hs Code.:

Synonyms:(3S,4R,5R,6R)-4,5-bis(benzyloxy)-6-(3'-hydroxy-(S)-1'-hydroxypropyl)-piperidin-3-yl pivalate

Suppliers and Price of (3S,4R,5R,6R)-4,5-bis(benzyloxy)-6-(3'-hydroxy-(S)-1'-hydroxypropyl)-piperidin-3-yl pivalate

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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 (3S,4R,5R,6R)-4,5-bis(benzyloxy)-6-(3'-hydroxy-(S)-1'-hydroxypropyl)-piperidin-3-yl pivalate

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Technology Process of (3S,4R,5R,6R)-4,5-bis(benzyloxy)-6-(3'-hydroxy-(S)-1'-hydroxypropyl)-piperidin-3-yl pivalate

There total 1 articles about (3S,4R,5R,6R)-4,5-bis(benzyloxy)-6-(3'-hydroxy-(S)-1'-hydroxypropyl)-piperidin-3-yl pivalate 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: 96.0%

: 1255955-56-6
(3S,4R,5R,6R)-4,5-bis(benzyloxy)-6-(3'-triisopropylsilanyloxy-(S)-1'-hydroxypropyl)-piperidin-3-yl pivalate

: 1255955-57-7
(3S,4R,5R,6R)-4,5-bis(benzyloxy)-6-(3'-hydroxy-(S)-1'-hydroxypropyl)-piperidin-3-yl pivalate

Guidance literature:: With tetrabutyl ammonium fluoride; In tetrahydrofuran; at 0 ℃; for 2h; Inert atmosphere;
DOI:10.1021/ol102371x

Reference yield:

: 1255955-57-7
(3S,4R,5R,6R)-4,5-bis(benzyloxy)-6-(3'-hydroxy-(S)-1'-hydroxypropyl)-piperidin-3-yl pivalate

: C₂₇H₃₆BrNO₅

Guidance literature:: With carbon tetrabromide; triethylamine; triphenylphosphine; In dichloromethane; at 0 - 20 ℃; for 3h; Inert atmosphere;
DOI:10.1021/ol102371x