33104-32-4

Basic information

• Product Name: β-(3-hydroxyphenyl)naphthalene
• Synonyms: β-(3-hydroxyphenyl)naphthalene
• CAS NO: 33104-32-4
• Molecular Weight: 220.271
• Mol File: 33104-32-4.mol
• Article Data: 10

Chemical Properties

• CAS DataBase Reference: β-(3-hydroxyphenyl)naphthalene(CAS DataBase Reference)
• NIST Chemistry Reference: β-(3-hydroxyphenyl)naphthalene(33104-32-4)
• EPA Substance Registry System: β-(3-hydroxyphenyl)naphthalene(33104-32-4)

Safety Data

• Hazardous Substances Data: 33104-32-4(Hazardous Substances Data)

Upstream product

• 42508-60-1 1-(2-oxopropyl)pyridinium chloride 
• 136539-66-7 3-diethylamino-1-[2]naphthyl-propan-1-one; hydrochloride 
• 33104-31-3 β-(3-methoxyphenyl)naphthalene 
• 580-13-2 2-bromonaphthalene 
• 10365-98-7 3-methoxyphenylboronic acid 
• 87199-18-6 3-hydroxyphenylboronic acid 
• 42160-93-0 3-(naphthalen-2-yl)cyclohex-2-en-1-one 
• 667940-23-0 2-(3-bromophenyl)naphthalene 
• 626-02-8 3-Iodophenol 
• 32316-92-0 naphthalene-2-boronic acid 
• 591-20-8 3-Bromophenol 

Downstream Products

• 933066-91-2 5-naphthalen-2-yl-2,2-diphenyl-2H-chromene 
• 933066-99-0 7-naphthalen-2-yl-2,2-diphenyl-2H-chromene 

Relevant articles and documents

Pd-catalyzed protecting-group-free cross-couplings of iodophenols with atom-economic triarylbismuth reagents

An efficient protocol for the protecting-group-free synthesis of unsymmetrical hydroxybiaryls via the Pd-catalyzed cross-couplings of unprotected iodophenols with triarylbismuth reagents is described. The presented protocols exhibits good to high yields of hydroxybiaryls.

AMINATION AND HYDROXYLATION OF ARYLMETAL COMPOUNDS

In one aspect, the present disclosure provides methods of preparing a primary or secondary amine and hydroxylated aromatic compounds. In some embodiments, the aromatic compound may be unsubstituted, substituted, or contain one or more heteroatoms within the rings of the aromatic compound. The methods described herein may be carried out without the need for transition metal catalysts or harsh reaction conditions.

An acetatopalladium(II) complex with 1-benzyl-N-(3,5-di-tert-butylsalicylidene)piperidin-4-amine: Synthesis, structure and catalytic applications in Suzuki–Miyaura coupling of arylboronic acids with hydroxyaryl halides

The Schiff base 1-benzyl-N-(3,5-di-tert-butylsalicylidene)piperidin-4-amine (HL) and its acetatopalladium(II) complex having the formula [Pd(L)(OAc)] were synthesized. Both HL and [Pd(L)(OAc)] were characterized using elemental analysis and various spectroscopic (infrared, UV–visible, 1H NMR and 13C NMR) and mass spectrometric measurements. The molecular structure of the complex was determined using X-ray crystallographic analysis. In the complex, the pincer-like NNO-donor L? and the monodenate OAc? provide a distorted square-planar N2O2 coordination environment around the metal centre. The physicochemical properties and the spectroscopic features of [Pd(L)(OAc)] are consistent with its molecular structure. The complex was found to be an effective catalyst for the Suzuki–Miyaura cross-coupling reactions of hydroxyaryl halides with arylboronic acids in predominantly aqueous media. The reactions afforded hydroxybiaryl products in good to excellent yields with a wide substrate scope.