tert-butyl 4-((5-amino-2-chlorophenoxy)methyl)piperidine-1-carboxylate

Base Information

Chemical Name:tert-butyl 4-((5-amino-2-chlorophenoxy)methyl)piperidine-1-carboxylate
CAS No.:1034491-93-4
Molecular Formula:C₁₇H₂₅ClN₂O₃
Molecular Weight:0
Hs Code.:
Mol file:1034491-93-4.mol

Synonyms:tert-butyl 4-((5-amino-2-chlorophenoxy)methyl)piperidine-1-carboxylate

Suppliers and Price of tert-butyl 4-((5-amino-2-chlorophenoxy)methyl)piperidine-1-carboxylate

Supply Marketing:

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

Manufacturers and distributors:

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Chemicals and raw materials
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Total 1 raw suppliers

Chemical Property of tert-butyl 4-((5-amino-2-chlorophenoxy)methyl)piperidine-1-carboxylate

Chemical Property:

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

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Technology Process of tert-butyl 4-((5-amino-2-chlorophenoxy)methyl)piperidine-1-carboxylate

There total 4 articles about tert-butyl 4-((5-amino-2-chlorophenoxy)methyl)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:

: 1034491-91-2
4-(2-chloro-5-nitro-phenoxymethyl)-piperidine-1-carboxylic acid tert-butyl ester

: 1034491-93-4
4-(5-amino-2-chloro-phenoxymethyl)-piperidine-1-carboxylic acid tert-butyl ester

Guidance literature:: With ethanol; tin(ll) chloride; at 70 - 80 ℃; for 5.5h;
DOI:10.1021/jm070034i

Reference yield:

: 1009-36-5
2-chloro-5-nitroanisole

: 1034491-93-4
4-(5-amino-2-chloro-phenoxymethyl)-piperidine-1-carboxylic acid tert-butyl ester

Guidance literature:: Multi-step reaction with 3 steps

1: HBr; acetic acid / 18 h / 140 °C

2: 5.59 mg / PPh₃; DIAD / tetrahydrofuran / 18 h / 20 °C

3: SnCl₂; ethanol / 5.5 h / 70 - 80 °C

With ethanol; di-isopropyl azodicarboxylate; hydrogen bromide; acetic acid; triphenylphosphine; tin(ll) chloride; In tetrahydrofuran; 2: Mitsunobu reaction;
DOI:10.1021/jm070034i

Reference yield:

: 619-10-3
5-nitro-2-chlorophenol

: 1034491-93-4
4-(5-amino-2-chloro-phenoxymethyl)-piperidine-1-carboxylic acid tert-butyl ester

Guidance literature:: Multi-step reaction with 2 steps

1: 5.59 mg / PPh₃; DIAD / tetrahydrofuran / 18 h / 20 °C

2: SnCl₂; ethanol / 5.5 h / 70 - 80 °C

With ethanol; di-isopropyl azodicarboxylate; triphenylphosphine; tin(ll) chloride; In tetrahydrofuran; 1: Mitsunobu reaction;
DOI:10.1021/jm070034i