Tert-butyl 4-hydroxy-4-(nitromethyl)piperidine-1-carboxylate

Base Information

• Chemical Name: Tert-butyl 4-hydroxy-4-(nitromethyl)piperidine-1-carboxylate
• CAS No.: 819800-93-6
• Molecular Formula: C11H20N2O5
• Molecular Weight: 260.29
• Hs Code.: 2933399990
• DSSTox Substance ID: DTXSID90704883
• Wikidata: Q82637456
• Mol file: 819800-93-6.mol

Synonyms:819800-93-6;tert-butyl 4-hydroxy-4-(nitromethyl)piperidine-1-carboxylate;1-Boc-4-hydroxy-4-(nitromethyl)piperidine;MFCD12963548;SCHEMBL1141077;DTXSID90704883;AJNCHUMJVPZDCG-UHFFFAOYSA-N;AKOS016000631;1-Piperidinecarboxylic acid, 4-hydroxy-4-(nitromethyl)-, 1,1-dimethylethyl ester;AC-23531;AS-73750;SY013364;CS-0243626;FT-0768811;EN300-266456;W16786;A916188;J-524708;Z1505695310;t-Butyl 4-hydroxy-4-(nitromethyl)piperidine-1-carboxylate;tert-butyl4-hydroxy-4-(nitromethyl)piperidine-1-carboxylate;4-Hydroxy-4-(nitromethyl)-1-piperidinecarboxylic acid 1,1-dimethylethyl ester

Chemical Property of Tert-butyl 4-hydroxy-4-(nitromethyl)piperidine-1-carboxylate

Chemical Property:

• PSA: 95.59000
• LogP: 1.48620
• XLogP3: 1.2
• Hydrogen Bond Donor Count: 1
• Hydrogen Bond Acceptor Count: 5
• Rotatable Bond Count: 3
• Exact Mass: 260.13722174
• Heavy Atom Count: 18
• Complexity: 323

Purity/Quality:

97% ^*data from raw suppliers

1-Boc-4-hydroxy-4-(nitromethyl)piperidine 95% ^*data from reagent suppliers

Safty Information:

• Pictogram(s):  
• Hazard Codes: 

MSDS Files:

SDS file from LookChem

Useful:

• Canonical SMILES: CC(C)(C)OC(=O)N1CCC(CC1)(C[N+](=O)[O-])O

Technology Process of Tert-butyl 4-hydroxy-4-(nitromethyl)piperidine-1-carboxylate

There total 3 articles about Tert-butyl 4-hydroxy-4-(nitromethyl)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: 98.0%

nitromethane (75-52-5) + N-tert-butyloxycarbonylpiperidin-4-one (79099-07-3) → tert-butyl 4-hydroxy-4-(nitromethyl)-piperidine-1-carboxylate (819800-93-6)

Guidance literature:

With sodium ethanolate; In ethanol; at 20 ℃;

Reference yield:

piperidin-4-one (41661-47-6) → tert-butyl 4-hydroxy-4-(nitromethyl)-piperidine-1-carboxylate (819800-93-6)

Guidance literature:

Multi-step reaction with 2 steps

1: sodium hydrogencarbonate / water / 50 °C

2: sodium methylate / methanol / 1 h / 20 °C

With sodium methylate; sodium hydrogencarbonate; In methanol; water;

Reference yield:

di-tert-butyl dicarbonate (24424-99-5) → tert-butyl 4-hydroxy-4-(nitromethyl)-piperidine-1-carboxylate (819800-93-6)

Guidance literature:

Multi-step reaction with 2 steps

1: sodium hydrogencarbonate / water / 50 °C

2: sodium methylate / methanol / 1 h / 20 °C

With sodium methylate; sodium hydrogencarbonate; In methanol; water;

upstream raw materials:

nitromethane

N-tert-butyloxycarbonylpiperidin-4-one

piperidin-4-one

di-tert-butyl dicarbonate

Downstream raw materials:

tert-butyl 3-oxo-1-oxa-4,9-diazaspiro[5.5]undecane-9-carboxylate

1-oxa-4,9-diazaspiro[5.5]undecane-9-carboxylic acid tert-butyl ester

4-aminomethyl-4-hydroxypiperidine-1-carboxylic acid tert-butyl ester