(4-methyl-benzyl)-piperidin-4-yl-carbamic acid benzyl ester hydrochloride

Base Information

Chemical Name:(4-methyl-benzyl)-piperidin-4-yl-carbamic acid benzyl ester hydrochloride
CAS No.:1091681-70-7
Molecular Formula:C₂₁H₂₆N₂O₂*ClH
Molecular Weight:374.911
Hs Code.:

Synonyms:(4-methyl-benzyl)-piperidin-4-yl-carbamic acid benzyl ester hydrochloride

Suppliers and Price of (4-methyl-benzyl)-piperidin-4-yl-carbamic acid benzyl ester hydrochloride

Supply Marketing:

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

Manufacturers and distributors:

Manufacture/Brand
Chemicals and raw materials
Packaging
price

Total 1 raw suppliers

Chemical Property of (4-methyl-benzyl)-piperidin-4-yl-carbamic acid benzyl ester hydrochloride

Chemical Property:

Purity/Quality:: 98% ^*data from raw suppliers

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:

Useful:

Technology Process of (4-methyl-benzyl)-piperidin-4-yl-carbamic acid benzyl ester hydrochloride

There total 3 articles about (4-methyl-benzyl)-piperidin-4-yl-carbamic acid benzyl ester hydrochloride 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:

: 104-87-0
4-methyl-benzaldehyde

: 1091681-70-7
(4-methyl-benzyl)-piperidin-4-yl-carbamic acid benzyl ester hydrochloride

Guidance literature:: Multi-step reaction with 3 steps

1: sodium tris(acetoxy)borohydride; acetic acid / 1,2-dichloro-ethane / 20 °C

2: sodium hydroxide / water; tetrahydrofuran / 20 °C

3: hydrogenchloride / water; ethyl acetate / 20 °C

With hydrogenchloride; sodium tris(acetoxy)borohydride; acetic acid; sodium hydroxide; In tetrahydrofuran; water; ethyl acetate; 1,2-dichloro-ethane;
DOI:10.1016/j.bmcl.2016.04.086

Reference yield:

: 87120-72-7
1-(tert-butoxycarbonyl)-4-aminopiperidine

: 1091681-70-7
(4-methyl-benzyl)-piperidin-4-yl-carbamic acid benzyl ester hydrochloride

Guidance literature:: Multi-step reaction with 3 steps

1: sodium tris(acetoxy)borohydride; acetic acid / 1,2-dichloro-ethane / 20 °C

2: sodium hydroxide / water; tetrahydrofuran / 20 °C

3: hydrogenchloride / water; ethyl acetate / 20 °C

With hydrogenchloride; sodium tris(acetoxy)borohydride; acetic acid; sodium hydroxide; In tetrahydrofuran; water; ethyl acetate; 1,2-dichloro-ethane;
DOI:10.1016/j.bmcl.2016.04.086

Reference yield:

: 359877-52-4
tert-butyl 4-((4-methylphenyl)methyl)aminopiperidine carboxylate

: 1091681-70-7
(4-methyl-benzyl)-piperidin-4-yl-carbamic acid benzyl ester hydrochloride

Guidance literature:: Multi-step reaction with 2 steps

1: sodium hydroxide / water; tetrahydrofuran / 20 °C

2: hydrogenchloride / water; ethyl acetate / 20 °C

With hydrogenchloride; sodium hydroxide; In tetrahydrofuran; water; ethyl acetate;
DOI:10.1016/j.bmcl.2016.04.086