cis-(3S)-hydroxy-(2S)-phenylpiperidine

Base Information

Chemical Name:cis-(3S)-hydroxy-(2S)-phenylpiperidine
CAS No.:148701-46-6
Molecular Formula:C₁₁H₁₅NO
Molecular Weight:177.246
Hs Code.:

Synonyms:cis-(3S)-hydroxy-(2S)-phenylpiperidine

Suppliers and Price of cis-(3S)-hydroxy-(2S)-phenylpiperidine

Supply Marketing:

Business phase:: The product has achieved commercial mass production^*data from LookChem market partment

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Total 1 raw suppliers

Chemical Property of cis-(3S)-hydroxy-(2S)-phenylpiperidine

Chemical Property:

Purity/Quality:: 97% ^*data from raw suppliers

Safty Information:

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Technology Process of cis-(3S)-hydroxy-(2S)-phenylpiperidine

There total 33 articles about cis-(3S)-hydroxy-(2S)-phenylpiperidine 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: 99.0%

: 159249-47-5
tert-butyl (2S,3S)-3-hydroxy-2-phenylpiperidine-1-carboxylate

: 148701-46-6
cis-(3S)-hydroxy-(2S)-phenylpiperidine

Guidance literature:: With trifluoroacetic acid; In dichloromethane;
DOI:10.1016/S0040-4039(99)01462-8

Reference yield: 96.0%

: 846044-72-2
(5S,6S)-5-hydroxy-6-phenylpiperidin-2-one

: 148701-46-6
cis-(3S)-hydroxy-(2S)-phenylpiperidine

Guidance literature:: (5S,6S)-5-hydroxy-6-phenylpiperidin-2-one; With borane-THF; for 5h; Inert atmosphere; Reflux;

With hydrogenchloride; In water; at 0 - 20 ℃; for 0.5h; Inert atmosphere;
DOI:10.1039/c2ob06644k

Reference yield:

: C₁₁H₁₅NO₂

: 148701-46-6
cis-(3S)-hydroxy-(2S)-phenylpiperidine

Guidance literature:: With 5% rhodium-on-charcoal; 20% palladium hydroxide-activated charcoal; hydrogen; In methanol; at 20 ℃; for 15h; under 7500.75 Torr; Autoclave;
DOI:10.1002/ejoc.201501333