Piperidine, 1-[(1-hydroxy-2-naphthalenyl)carbonyl]-

Base Information

• Chemical Name: Piperidine, 1-[(1-hydroxy-2-naphthalenyl)carbonyl]-
• CAS No.: 29777-42-2
• Molecular Formula: C16H17 N O2
• Molecular Weight: 255.316
• European Community (EC) Number: 249-841-7
• NSC Number: 158016
• UNII: N9HE2LA3B2
• DSSTox Substance ID: DTXSID4067511
• Nikkaji Number: J286.959D
• Wikidata: Q81994117
• ChEMBL ID: CHEMBL1981468
• Mol file: 29777-42-2.mol

Synonyms:29777-42-2;1-Hydroxy-2-naphthopiperidide;Piperidine, 1-[(1-hydroxy-2-naphthalenyl)carbonyl]-;Piperidine, 1-(1-hydroxy-2-naphthoyl)-;1-Hydroxy-2-naphthoic acid piperidide;(1-hydroxynaphthalen-2-yl)-piperidin-1-ylmethanone;N9HE2LA3B2;1-[(1-HYDROXY-2-NAPHTHYL)CARBONYL]PIPERIDINE;MLS002920687;EINECS 249-841-7;Methanone, (1-hydroxy-2-naphthalenyl)-1-piperidinyl-;Piperidine, 1-((1-hydroxy-2-naphthalenyl)carbonyl)-;NSC 158016;NSC-158016;1-((1-Hydroxy-2-naphthyl)carbonyl)piperidine;NSC158016;UNII-N9HE2LA3B2;CHEMBL1981468;DTXSID4067511;SCHEMBL11335881;AKOS000207645;NCI60_001156;SMR001798274;(1-HYDROXY-2-NAPHTHALENYL)-1-PIPERIDINYLMETHANONE

Chemical Property of Piperidine, 1-[(1-hydroxy-2-naphthalenyl)carbonyl]-

Chemical Property:

• Vapor Pressure: 2.35E-09mmHg at 25°C
• Boiling Point: 467.3°Cat760mmHg
• Flash Point: 236.4°C
• PSA: 40.54000
• Density: 1.232g/cm³
• LogP: 3.10940
• XLogP3: 3.7
• Hydrogen Bond Donor Count: 1
• Hydrogen Bond Acceptor Count: 2
• Rotatable Bond Count: 1
• Exact Mass: 255.125928785
• Heavy Atom Count: 19
• Complexity: 325

Purity/Quality:

99% ^*data from raw suppliers

Safty Information:

• Pictogram(s):  
• Hazard Codes: 

MSDS Files:

SDS file from LookChem

Useful:

• Canonical SMILES: C1CCN(CC1)C(=O)C2=C(C3=CC=CC=C3C=C2)O

Technology Process of Piperidine, 1-[(1-hydroxy-2-naphthalenyl)carbonyl]-

There total 4 articles about Piperidine, 1-[(1-hydroxy-2-naphthalenyl)carbonyl]- 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:

piperidine (110-89-4) + 1-hydroxy-2-naphthoyl chloride (38077-69-9) → (1-hydroxynaphthalen-2-yl)(piperidin-1-yl)methanone (29777-42-2) + 2-(piperidine-1-carbonyl)naphthalen-1-yl 1-hydroxy-2-naphthoate (1388147-00-9)

Guidance literature:

With N-ethyl-N,N-diisopropylamine; In dichloromethane; at 0 - 20 ℃;

DOI:10.1016/j.dyepig.2011.07.013

Reference yield:

1-hydroxy-2-naphthoic acid (86-48-6) → (1-hydroxynaphthalen-2-yl)(piperidin-1-yl)methanone (29777-42-2) + 2-(piperidine-1-carbonyl)naphthalen-1-yl 1-hydroxy-2-naphthoate (1388147-00-9)

Guidance literature:

Multi-step reaction with 2 steps

1: thionyl chloride / n-heptane; N,N-dimethyl-formamide / 4 h / Reflux

2: N-ethyl-N,N-diisopropylamine / dichloromethane / 0 - 20 °C

With thionyl chloride; N-ethyl-N,N-diisopropylamine; In n-heptane; dichloromethane; N,N-dimethyl-formamide;

DOI:10.1016/j.dyepig.2011.07.013

Reference yield:

1-hydroxy-2-naphthoic acid (86-48-6) → (1-hydroxynaphthalen-2-yl)(piperidin-1-yl)methanone (29777-42-2) + (4-chloro-1-hydroxynaphthalen-2-yl)(piperidin-1-yl)methanone (1388146-98-2) + 2-(piperidine-1-carbonyl)naphthalen-1-yl 1-hydroxy-2-naphthoate (1388147-00-9)

Guidance literature:

Multi-step reaction with 2 steps

1: thionyl chloride / n-heptane; N,N-dimethyl-formamide / 4 h / Reflux

2: dichloromethane / 0 - 20 °C

With thionyl chloride; In n-heptane; dichloromethane; N,N-dimethyl-formamide;

DOI:10.1016/j.dyepig.2011.07.013

upstream raw materials:

piperidine

1-hydroxy-2-naphthoyl chloride

1-hydroxy-2-naphthoic acid

Downstream raw materials:

(1-hydroxy-4-(phenyldiazenyl)naphthalen-2-yl)(piperidin-1-yl)methanone

Refernces