تفاعل #996916
ord-cf5c687de4c24f34b945268b13918e86
معادلة التفاعل
المتفاعلات
ظروف التفاعل
المعالجة
- 1أخرىThe solvent was removed in vacuo
- 2أخرىthe residue was dried
- 3workup.STIRRINGstirred
- 4درجة الحرارةthe mixture was then cooled by means of an ice-bath
- 5أخرىthe ice bath was removed
- 6workup.STIRRINGthe reaction mixture was stirred at room temperature for 72 h
- 7أخرىCompounds were separated via flash chromatography on silica gel column
الإجراء التجريبي
A mixture of (R,R)-(−)-N,N′-Bis(3,5-di-tert-butylsalicylidene)-1,2-cyclohexane diaminocobalt (II) (0.22 g, 0.37 mmol, 0.8%), toluene (5 ml), and acetic acid (0.044 g, 0.74 mmol) was stirred for 1 h at room temperature. The solvent was removed in vacuo and the residue was dried. 2-Benzhydryl-oxirane (9.6 g, 45.7 mmol) was added in one portion and stirred, the mixture was then cooled by means of an ice-bath. H2O (0.58 g, 32 mmol) was slowly added over a 30-min period. After water addition, the ice bath was removed and the reaction mixture was stirred at room temperature for 72 h. Compounds were separated via flash chromatography on silica gel column to give (2R)-2-benzhydryl-oxirane (23a) 4.5 g ([α]D=(+)9.58, c=1, MeOH) and (2S)-3,3-diphenyl-propane-1,2-diol 24 3.53 g ([α]D=(+)48, c=1, MeOH, ee=97%). The proton and carbon NMR data of (2R)-2-benzhydryl-oxirane was identical to the racemate 2-benzhydryl-oxirane.