1-BOC-4-[AMINO(4-CHLOROPHENYL)METHYL]-PIPERIDINE

Base Information

Chemical Name:1-BOC-4-[AMINO(4-CHLOROPHENYL)METHYL]-PIPERIDINE
CAS No.:885595-32-4
Molecular Formula:C17H25ClN2O2
Molecular Weight:324.851
Hs Code.:
Mol file:885595-32-4.mol

Synonyms:4-[amino-(4-chlorophenyl)methyl]piperidine-1-carboxylic acid tert-butyl ester;

Suppliers and Price of 1-BOC-4-[AMINO(4-CHLOROPHENYL)METHYL]-PIPERIDINE

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 1-BOC-4-[AMINO(4-CHLOROPHENYL)METHYL]-PIPERIDINE

Chemical Property:

PSA：55.56000
LogP:4.62510

Purity/Quality:

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:

Useful:

Technology Process of 1-BOC-4-[AMINO(4-CHLOROPHENYL)METHYL]-PIPERIDINE

There total 4 articles about 1-BOC-4-[AMINO(4-CHLOROPHENYL)METHYL]-PIPERIDINE 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: 82.0%

: 209808-06-0
tert-butyl 4-(4-chlorobenzoyl)piperidine-1-carboxylate

: 885595-32-4
4-[amino(4-chlorophenyl)methyl]piperidine-1-carboxylic acid tert-butyl ester

Guidance literature:: tert-butyl 4-(4-chlorobenzoyl)piperidine-1-carboxylate; With ammonium acetate; sodium cyanoborohydride; In methanol; at 20 ℃; for 20h;

With sodium hydroxide; In water;

Reference yield: 79.0%

: 918501-87-8
C₁₇H₂₃ClN₄O₂

: 885595-32-4
4-[amino(4-chlorophenyl)methyl]piperidine-1-carboxylic acid tert-butyl ester

Guidance literature:: With triphenylphosphine; In tetrahydrofuran; water; for 16h; Heating / reflux;

Reference yield:

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

: 885595-32-4
4-[amino(4-chlorophenyl)methyl]piperidine-1-carboxylic acid tert-butyl ester

Guidance literature:: Multi-step reaction with 2 steps

1: triethylamine / acetonitrile / 16 h / 20 °C

2: ammonium acetate; sodium cyanoborohydride / methanol / 20 h / 20 °C / Heating / reflux

With ammonium acetate; sodium cyanoborohydride; triethylamine; In methanol; acetonitrile;