18531-99-2

Basic information

• Product Name: (S)-(-)-1,1'-Bi-2-naphthol
• Synonyms: (s)-(-)-1,1’-bi-2-nanphthol;(R)-(+)-2,2'-DIHYDROXY-1,1'-BINAPHTHYL;(R)-(+)-2,2'-DIHYDROXY-1,1-BINAPHTHYL;(R)-(+)-1,1'-BI(2,2'-NAPHTHOL);(R)-(+)-1,1'-BINAPHTHYL-2,2'-DIOL;R(+)-1,1'-BINAPHTHALENE-2,2'-DIOL;(R)-[1,1]-BINAPHTHALENYL-2,2'-DIOL;(R)-(+)-1,1'-BIS(2-NAPHTHOL)
• CAS NO: 18531-99-2
• Molecular Formula: C₂₀H₁₄O₂
• Molecular Weight: 286.32
• EINECS: 210-014-0
• Product Categories: Intermediates of Dyes and Pigments;blocks;BuildingBlocks;Alcohols and Derivatives;chiral;CHIRAL COMPOUNDS;Chiral Reagent;Asymmetric Synthesis;Synthetic Organic Chemistry;Chiral Compound;Peptide;BINOL Series;Chiral Oxygen
• Mol File: 18531-99-2.mol
• Article Data: 139

Chemical Properties

• Melting Point: 215-218 °C
• Boiling Point: 388.69°C (rough estimate)
• Appearance: White to light gray/Crystals or Crystalline Powder
• Density: 1 g/cm3
• Refractive Index: -36.0 ° (C=1, THF)
• Storage Temp.: 2-8°C
• Solubility: dioxane: 50 mg/mL, clear
• PKA: 8.29±0.50(Predicted)
• Merck: 14,1226
• BRN: 3592999
• CAS DataBase Reference: (S)-(-)-1,1'-Bi-2-naphthol(CAS DataBase Reference)
• NIST Chemistry Reference: (S)-(-)-1,1'-Bi-2-naphthol(18531-99-2)
• EPA Substance Registry System: (S)-(-)-1,1'-Bi-2-naphthol(18531-99-2)

Safety Data

• Hazard Codes: T,Xi
• Statements: 25-36-36/37/38
• Safety Statements: 26-45-24/25-36
• RIDADR: UN 2811 6.1/PG 3
• WGK Germany: 3
• RTECS: DU3106100
• F: 10
• TSCA: No
• HazardClass: 6.1
• PackingGroup: III
• Hazardous Substances Data: 18531-99-2(Hazardous Substances Data)

Usage

Chemical Properties

white to light yellow crystal powde

Uses

Different sources of media describe the Uses of 18531-99-2 differently. You can refer to the following data:
1. Chiral ligand.
2. (S)-BINOL ligand in combination with titanium(IV) isopropoxide, forms (S)-(-)-BINOL-Ti complex, which is an effective chiral catalyst for:asymmetric addition of alkynylzinc to unactivated ketonesenantioselective ring-opening reaction of meso-stilbene oxide and cyclohexene oxide with anilinesasymmetric aryl transfers from triaryl(tetrahydrofuran)aluminum reagents to a wide variety of ketonesIt can also react with zirconium(IV) isopropoxide isopropanol complex to form a chiral Lewis acid catalyst for the facile enantioselective allylation of aldehydes by allyltributyltin.

Upstream product

• 100569-82-2 2,2'-diacetoxy-1,1'-binaphthyl 
• 6351-10-6 1-Indanol 
• 100465-50-7 <1,1'-Binaphthalene>-2,2'-diol dibutanoate 
• 124040-95-5 <1,1'-Binaphthalene>-2,2'-diol butanoate 
• 100465-49-4 <1,1'-Binaphthalene>-2,2'-diol dipropanoate 
• 80409-66-1 (+)-(S)-2'-hydroxy-2-(hydroxymethyl)-1,1'-binaphthyl 
• 18531-96-9 (S)-1,1'-binaphthyl-2,2'-dicarboxylic acid 
• 100465-52-9 <1,1'-Binaphthalene>-2,2'-diol dihexanoate 
• 121073-29-8 <1,1'-Binaphthalene>-2,2'-diol diheptanoate 
• 121073-30-1 <1,1'-Binaphthalene>-2,2'-diol dioctanoate 
• 100465-51-8 <1,1'-Binaphthalene>-2,2'-diol dipentanoate 
• 77196-14-6 (SS)-tetranaphtho<2,1-b:1,2-d:1,2-h:1,2-j><1,6>dioxacyclododeca-2,4,8,10-tetraene-7,12-dione 
• 77196-14-6 C₄₂H₂₄O₄ 
• 135-19-3 β-naphthol 

Downstream Products

• 121123-20-4 C₂₀H₁₄O₂*C₈H₁₁NOS 
• 121123-20-4 C₂₀H₁₄O₂*C₈H₁₁NOS 
• 2960-93-2 (-)-2,2'-Dimethoxy-1,1'-binaphthalene 
• 124931-84-6 p-Tolyl-acetic acid 2'-hydroxy-[1,1']binaphthalenyl-2-yl ester 
• 124931-83-5 (2-Methoxy-phenyl)-acetic acid 2'-hydroxy-[1,1']binaphthalenyl-2-yl ester 
• 74292-20-9 (S)-2,2'-bis(methoxymethoxy)-1,1'-binaphthyl 
• 911822-61-2 (S)-2,2'-bis(2-bromo-3,4,5-trimethoxybenzoyl)-1,1'-binaphthalene 
• 124931-82-4 4-Methoxyphenylacetic acid (S)-(-)-2'-hydroxy-1,1'-binaphthyl-2-yl ester 
• 124931-85-7 (4-Chloro-phenyl)-acetic acid 2'-hydroxy-[1,1']binaphthalenyl-2-yl ester 
• 75640-87-8 (S)-2,2'-dimethoxy-1,1'-dinaphthyl 
• 128544-06-9 (S)-(+)-2,2'-bis(p-toluenesulfonyloxy)-1,1'-binaphthalene 
• 157364-93-7 2'-hydroxy-1,1'-binaphthalen-2-yl benzoylformate 

Relevant articles and documents

One-pot preparation of chiral dinuclear vanadium(V) complex

A convenient one-pot procedure for the preparation of dinuclear vanadium(V) complex is described. The complex exhibited high catalytic activity for oxidative coupling of 2-naphthol derivatives. In addition, coupling of 9-phenanthrol gave (S)-10,10′-dihydroxy-9,9′-biphenanthryl in quantitative yield with 93% ee. Georg Thieme Verlag Stuttgart.

Enantioselective, Electrocatalytic Oxidative Coupling of Naphthol, Naphthyl Ether and Phenanthrol on a TEMPO-modified Graphite Felt Electrode in the Presence of (-)-Sparteine (TEMPO = 2,2,6,6-tetramethylpiperidin-1-yloxyl)

Constant potential electrolysis of 2-naphthol, 2-methoxynaphthalene and 10-hydroxyphenanthrene at 0.6 V vs.Ag/AgCl on a TEMPO-modified graphite felt electrode in the presence of (-)-sparteine in acetonitrile yields, enantioselectively, (S)-binaphthyl type dimers in > 92percent isolated yield and with > 88percent current efficiency with enantiomeric excess of 98, 91 and 97percent respectively for each dimer, respectively.

Thermal racemization of biaryl atropisomers

Many biaryl compounds possess atropisomerism due to the steric hindrance of substituents at the ortho-position of the two aromatic moieties. Upon heating, atropisomers may have enough energy to surpass the rotational energy barrier and racemize. The thermal stability of five atropisomers was studied using chiral chromatography by following the change in enantiomeric excess ratio at different temperatures. The first order racemization reaction rate was obtained at a given temperature as the slope of the change in enantiomeric excess ratio versus time. For each atropisomer, the racemization rates at different temperatures led to the value of the rotational energy barrier for racemization, ΔG?, and to the racemization half lifetime, t1/2, indicating the atropisomer thermal stability. Binaphthol started to racemize significantly at temperature of 190 °C and above while binaphthyldiamine was much more stable showing little or very minor racemization up to 210 °C. A chloro-substituted phenylamino-naphthol was very sensitive to thermal racemization starting at a low 40 °C.

Catalytic enantioselective synthesis of atropisomeric biaryls by a cation-directed O-alkylation

Axially chiral biaryls, as exemplified by 1,1′-bi-2-naphthol (BINOL), are key components of catalysts, natural products and medicines. These materials are synthesized conventionally in enantioenriched form through metal-mediated cross coupling, de novo construction of an aromatic ring, point-to-axial chirality transfer or an atropselective transformation of an existing biaryl. Here, we report a highly enantioselective organocatalytic method for the synthesis of atropisomeric biaryls by a cation-directed O-alkylation. Treatment of racemic 1-aryl-2-tetralones with a chiral quinidine-derived ammonium salt under basic conditions in the presence of an alkylating agent leads to atropselective O-alkylation with e.r. up to 98:2. Oxidation with DDQ gives access to C 2 -symmetric and non-symmetric BINOL derivatives without compromising e.r. We propose that the chiral ammonium counterion differentiates between rapidly equilibrating atropisomeric enolates, leading to highly atropselective O-alkylation. This dynamic kinetic resolution process offers a general approach to the synthesis of enantioenriched atropisomeric materials.

Chiral separation materials based on derivatives of 6-amino-6-deoxyamylose

In order to develop new type of chiral separation materials, in this study, 6-amino-6-deoxyamylose was used as chiral starting material with which 10 derivatives were synthesized. The amino group in 6-amino-6-deoxyamylose was selectively acylated and then the hydroxyl groups were carbamoylated yielding amylose 6-amido-6-deoxy-2,3-bis(phenylcarbamate)s, which were employed as chiral selectors (CSs) for chiral stationary phases of high-performance liquid chromatography. The resulted 6-amido-6-deoxyamyloses and amylose 6-amido-6-deoxy-2,3-bis(phenylcarbamate)s were characterized by IR, 1H NMR, and elemental analysis. Enantioseparation evaluations indicated that most of the CSs demonstrated a moderate chiral recognition capability. The 6-nonphenyl (6-nonPh) CS of amylose 6-cyclohexylformamido-6-deoxy-2,3-bis(3,5-dimethylphenylcarbamate) showed the highest enantioselectivity towards the tested chiral analytes; the phenyl-heterogeneous (Ph-hetero) CS of amylose 6-(4-methylbenzamido)-6-deoxy-2,3-bis(3,5-dimethylphenylcarbamate) baseline separated the most chiral analytes; the phenyl-homogeneous (Ph-homo) CS of amylose 6-(3,5-dimethylbenzamido)-6-deoxy-2,3-bis(3,5-dimethylphenylcarbamate) also exhibited a good enantioseparation capability among the developed CSs. Regarding Ph-hetero CSs, the enantioselectivity depended on the combination of the substituent at 6-position and that at 2- and 3-positions; as for Ph-homo CSs, the enantioselectivity was related to the substituent at 2-, 3-, and 6-positions; with respect to 6-nonPh CSs, the retention factor of most analytes on the corresponding CSPs was lower than that on Ph-hetero and Ph-homo CSPs in the same mobile phases, indicating π–π interactions did occur during enantioseparation. Although the substituent at 6-position could not provide π–π interactions, the 6-nonPh CSs demonstrated an equivalent or even higher enantioselectivity compared with the Ph-homo and Ph-hetero CSs.

Enantiodivergent Kinetic Resolution of 1,1′-Biaryl-2,2′-Diols and Amino Alcohols by Dipeptide-Phosphonium Salt Catalysis Inspired by the Atherton–Todd Reaction

A highly enantiodivergent organocatalytic method is disclosed for the synthesis of atropisomeric biaryls via kinetic resolution inspired by a dipeptide-phosphonium salt-catalyzed Atherton–Todd (A-T) reaction. This flexible approach led to both R- and S-enantiomers by fine-tuning of bifunctional phosphonium with excellent selectivity factors (s) of up to 1057 and 525, respectively. The potential of newly synthesized O-phosphorylated biaryl diols was illustrated by the synthesis of axially chiral organophosphorus compounds. Mechanistic investigations suggest that the bifunctional phosphonium halide catalyst differentiates between the in-situ-generated P-species in the A-T process, mainly involving phosphoryl chloride and phosphoric anhydride, thus leading to highly enantiodivergent O-phosphorylation reactions. Furthermore hydrogen bonding interactions between the catalysts and phosphorus molecules were crucial in asymmetric induction.