(S)-(-)-Di-(2-naphthyl)-2-pyrrolidinemethanol

CAS : 127986-84-9

Ref. 3D-FD147847

Informations sur le produit

• Nom: (S)-(-)-Di-(2-naphthyl)-2-pyrrolidinemethanol
• Synonymes: (S)-(-)-Alpha,Alpha-Di(2-Napthyl)-2-Pyrrolidinemethanol, (S)-(-)-Di-(2-Naphthyl)-2-Pyrrolidinemethanol, (S)-Di-2-Naphthylprolinol, (S)-Di-2-Naphthylprolinol 99%, (S)-(-)-A,A-Di(2-Naphthyl)-2-Pyrrolidinemethanol, dinaphthalen-2-yl[(2S)-pyrrolidin-2-yl]methanol, (2R)-2-[hydroxy(dinaphthalen-2-yl)methyl]pyrrolidinium, (2S)-2-[hydroxy(dinaphthalen-2-yl)methyl]pyrrolidinium

Description

The synthesis of (S)-(-)-Di-(2-naphthyl)-2-pyrrolidinemethanol is a two-step process that begins with the epoxidation of tert-butanol. This reaction produces an epoxide, which is then condensed with 2-naphthol to form the desired product. The carbonyl group in this molecule is chiral, which means that it can be resolved into two enantiomers. The use of a chiral selector allows for the selective formation of one enantiomer over the other. Epoxidation reactions can be carried out in organic solvents, such as dichloromethane, chloroform, and tert-butyl alcohol. These reactions are typically carried out at room temperature for 10 hours or less and require catalytic amounts of oxidant. Preparative methods may also be used to produce racemic mixtures or pure enantiomers.

• Marque: Biosynth

Propriétés chimiques

• Masse moléculaire: 353.46 g/mol
• Formule: C₂₅H₂₃NO
• Degré de pureté: Min. 95%
• InChI: InChI=1S/C25H23NO/c27-25(24-10-5-15-26-24,22-13-11-18-6-1-3-8-20(18)16-22)23-14-12-19-7-2-4-9-21(19)17-23/h1-4,6-9,11-14,16-17,24,26-27H,5,10,15H2/t24-/m0/s1
• Code InChI: InChIKey=LNUDNNFEXRHHGY-DEOSSOPVSA-N
• SMILES: OC(c1ccc2ccccc2c1)(c1ccc2ccccc2c1)[C@@H]1CCCN1