benzyl (3R,4R)-4-(benzhydrylideneamino)-3-hydroxy-piperidine-1-carboxylate

Base Information

Chemical Name:benzyl (3R,4R)-4-(benzhydrylideneamino)-3-hydroxy-piperidine-1-carboxylate
CAS No.:1007596-64-6
Molecular Formula:C₂₆H₂₆N₂O₃
Molecular Weight:414.504
Hs Code.:

Synonyms:benzyl (3R,4R)-4-(benzhydrylideneamino)-3-hydroxy-piperidine-1-carboxylate

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Chemical Property of benzyl (3R,4R)-4-(benzhydrylideneamino)-3-hydroxy-piperidine-1-carboxylate

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Technology Process of benzyl (3R,4R)-4-(benzhydrylideneamino)-3-hydroxy-piperidine-1-carboxylate

There total 3 articles about benzyl (3R,4R)-4-(benzhydrylideneamino)-3-hydroxy-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: 93.0%

: 1013-88-3
Benzophenone imine

: 959617-87-9
benzyl (3R,4R)-4-amino-3-hydroxy-piperidine-1-carboxylate

: 1007596-64-6
benzyl (3R,4R)-4-(benzhydrylideneamino)-3-hydroxy-piperidine-1-carboxylate

Guidance literature:: In toluene; for 12h; Reflux;
DOI:10.1021/jm500462x

Reference yield:

: 167832-25-9
trans(±)benzyl-4-azido-3-hydroxypiperidine-1-carboxylate

: 1007596-64-6
benzyl (3R,4R)-4-(benzhydrylideneamino)-3-hydroxy-piperidine-1-carboxylate

Guidance literature:: Multi-step reaction with 3 steps

1.1: triphenylphosphine / tetrahydrofuran / 2 h / 20 °C

1.2: 20 °C

2.1: chiral column Column: AD 250 / Resolution of racemate

3.1: toluene / 12 h / Reflux

With triphenylphosphine; In tetrahydrofuran; toluene;
DOI:10.1021/jm500462x

Reference yield:

: (+/-)-trans-benzyl 4-amino-3-hydroxypiperdine-1-carboxylate

: 1007596-64-6
benzyl (3R,4R)-4-(benzhydrylideneamino)-3-hydroxy-piperidine-1-carboxylate

Guidance literature:: Multi-step reaction with 2 steps

1: chiral column Column: AD 250 / Resolution of racemate

2: toluene / 12 h / Reflux

With chiral column Column: AD 250; In toluene;
DOI:10.1021/jm500462x